松原 誠二郎

Last Update: 2015/06/09 14:10:16

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Name(Kanji/Kana/Abecedarium Latinum)
松原 誠二郎/マツバラ セイジロウ/Matsubara, Seijiro
Primary Affiliation(Org1/Job title)
Graduate Schools Engineering/Professor
Faculty
Org1 Job title
工学部
Contact Address
Type Address(Japanese) Address(English)
Office 〒615-8510 京都府京都市西京区京大桂A-クラスター Kyoudai-katsura A-Cluster Nishikyo, Kyoto 615-8510
Phone
Type Number
Office 075-383-7130
E-mail Address
matsubara.seijiro.2e @ kyoto-u.ac.jp
Academic Organizations You are Affiliated to in Japan
Organization name(Japanese) Organization name(English)
日本化学会
有機合成化学協会
近畿化学協会
希土類学会
Academic Degree
Field(Japanese) Field(English) University(Japanese) University(English) Method
工学修士 京都大学
工学博士 京都大学
Graduate School
University(Japanese) University(English) Faculty(Japanese) Faculty(English) Major(Japanese) Major(English) Degree
京都大学 大学院工学研究科博士後期課程工業化学専攻 修了
京都大学 大学院工学研究科修士課程工業化学専攻 修了
Undergraduate School / Major(s)
University(Japanese) University(English) Faculty(Japanese) Faculty(English) Major(s)(Japanese) Major(s)(English) Degree
京都大学 工学部工業化学科 卒業
High School
Highschool Kana
私立六甲学院高校 しりつろっこうがくいんこうこう
Work Experience
Period Organization(Japanese) Organization(English) Job title(Japanese) Job title(English)
1986/04/01-1995/03/31 京都大学工学部 Kyoto University, Faculty of Engineering 助手 Assistant Professor
1988/09/01-1989/08/31 スタンフォード大学化学科 Stanford University, Department of Chemistry 博士研究員 Postdoctoral Fellow
1995/04/01-2005/12/31 京都大学大学院工学研究科 Kyoto University, Graduate School of Engineering 助教授 Associate Professor
2006/01/01- 京都大学大学院工学研究科 Kyoto University, Graduate School of Engineering 教授 Professor
Language of Instruction
Language(japanese) Language(english) Code
英語
Personal Website(s) (URL(s))
URL
http://www.dfm.kuic.kyoto-u.ac.jp/Website/Welcome.html
researchmap URL
https://researchmap.jp/read0012787
Fields of research (key words)
Key words(Japanese) Key words(English)
有機遷移金属反応剤を用いる高選択的合成反応の開発 Development of a highly selective syntheses by organo-transition-metallic reagents
有機典型金属反応剤を用いる高選択的合成反応の開発 Development of a highly selective syntheses by organo-main-metallic reagents
有機分子触媒を用いる高選択的合成反応の開発 Development of a highly selective syntheses by organocatalyst
Published Papers
Author Author(Japanese) Author(English) Title Title(Japanese) Title(English) Bibliography Bibliography(Japanese) Bibliography(English) Publication date Refereed paper Language Publishing type Disclose
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro Asymmetric syn-1,3-Dioxane Construction via Kinetic Resolution of Secondary Alcohols Using Chiral Phosphoric Acid Catalysts Asymmetric syn-1,3-Dioxane Construction via Kinetic Resolution of Secondary Alcohols Using Chiral Phosphoric Acid Catalysts Asymmetric syn-1,3-Dioxane Construction via Kinetic Resolution of Secondary Alcohols Using Chiral Phosphoric Acid Catalysts Asia, 8, 6, 814-818 Asian J. Org. Chem., 8, 6, 814-818 Asia, 8, 6, 814-818 2019/06 Refereed English Disclose to all
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes Cationic Cobalt Porphyrin-Catalyzed Allylation of Aldehydes with Allyltrimethylsilanes Org. Lett., 21, 10, 3834-3837 Org. Lett., 21, 10, 3834-3837 Org. Lett., 21, 10, 3834-3837 2019/05 Refereed Disclose to all
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro Asymmetric Aza‐Diels–Alder Reaction with Ion‐Paired – Iron Lewis Acid – Brønsted Acid Catalyst Asymmetric Aza‐Diels–Alder Reaction with Ion‐Paired – Iron Lewis Acid – Brønsted Acid Catalyst Asymmetric Aza‐Diels–Alder Reaction with Ion‐Paired – Iron Lewis Acid – Brønsted Acid Catalyst Chem.—Eur. J., 25, 38, 8987-8991 Chem.—Eur. J., 25, 38, 8987-8991 Chem.—Eur. J., 25, 38, 8987-8991 2019/05 Refereed Disclose to all
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers Org. Lett., 21, 7, 2156-2160 Org. Lett., 21, 7, 2156-2160 Org. Lett., 21, 7, 2156-2160 2019/04 Refereed English Research paper(scientific journal) Disclose to all
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro Organocatalytic Enantio- and Diastereoselective Construction of syn-1,3-Diol Motifs via Dynamic Kinetic Resolution of In Situ Generated Chiral Cyanohydrins Organocatalytic Enantio- and Diastereoselective Construction of syn-1,3-Diol Motifs via Dynamic Kinetic Resolution of In Situ Generated Chiral Cyanohydrins Organocatalytic Enantio- and Diastereoselective Construction of syn-1,3-Diol Motifs via Dynamic Kinetic Resolution of In Situ Generated Chiral Cyanohydrins Org. Lett., 21, 8, 2688-2692 Org. Lett., 21, 8, 2688-2692 Org. Lett., 21, 8, 2688-2692 2019/04 Refereed Disclose to all
松原 誠二郎 松原 誠二郎 反応集積化と中分子合成――新しい合成手法の開発 反応集積化と中分子合成――新しい合成手法の開発 化学と工業 , 21, 2, 121-123 化学と工業 , 21, 2, 121-123 , 21, 2, 121-123 2019/02 Refereed Japanese Research paper(scientific journal) Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA Kinetic Resolution of Acylsilane Cyanohydrins via Organocatalytic Cycloetherification Kinetic Resolution of Acylsilane Cyanohydrins via Organocatalytic Cycloetherification Chem.—Asian J. , 14, 116-120 Chem.—Asian J. , 14, 116-120 , 14, 116-120 2019/01 Refereed English Disclose to all
Yumi Kato, Craig A. Williams, Masanobu Uchiyama, Seijiro MATSUBARA Yumi Kato, Craig A. Williams, Masanobu Uchiyama, Seijiro MATSUBARA A Protocol for an Iodine–Metal Exchange Reaction on Cubane Using Lithium Organozincates A Protocol for an Iodine–Metal Exchange Reaction on Cubane Using Lithium Organozincates Org. Lett., 21, 2, 473-475 Org. Lett., 21, 2, 473-475 , 21, 2, 473-475 2019/01 Refereed English Disclose to all
Seijiro MATSUBARA Seijiro MATSUBARA H/D Exchange Using Hot Heavy Water H/D Exchange Using Hot Heavy Water Chimia , 72, 853-858 Chimia , 72, 853-858 , 72, 853-858 2018/12 Refereed English Disclose to all
松原 誠二郎、寺山慧、奥野恭史 松原 誠二郎、寺山慧、奥野恭史 コンピュータ支援有機合成の現在 コンピュータ支援有機合成の現在 MedChem News, 28, 4, 181-189 MedChem News, 28, 4, 181-189 , 28, 4, 181-189 2018/11 Refereed Disclose to all
Takuya Kurahashi, Seijiro MATSUBARA Takuya Kurahashi, Seijiro MATSUBARA Nickel-catalyzed Intermolecular Carboiodination of Alkynes with Aryl Iodides Nickel-catalyzed Intermolecular Carboiodination of Alkynes with Aryl Iodides Chem. Commun. , 54, 12750-12753 Chem. Commun. , 54, 12750-12753 , 54, 12750-12753 2018/11 Refereed English Disclose to all
Takuya Kurahashi, Seijiro MATSUBARA Takuya Kurahashi, Seijiro MATSUBARA FeCl3 as an Ion-Pairing Lewis Acid Catalyst. Formation of Highly Lewis Acidic FeCl2+ and Thermodynamically Stable FeCl4– To Catalyze the Aza-Diels–Alder Reaction with High Turnover Frequency FeCl3 as an Ion-Pairing Lewis Acid Catalyst. Formation of Highly Lewis Acidic FeCl2+ and Thermodynamically Stable FeCl4– To Catalyze the Aza-Diels–Alder Reaction with High Turnover Frequency Org. Lett. , 20, 7474-7477 Org. Lett. , 20, 7474-7477 , 20, 7474-7477 2018/11 Refereed English Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA trans‐Cyclooctenes as Halolactonization Catalysts trans‐Cyclooctenes as Halolactonization Catalysts Angew. Chem., Int. Ed., 57, 13863-13867 Angew. Chem., Int. Ed., 57, 13863-13867 , 57, 13863-13867 2018/10 Refereed English Disclose to all
Keisuke Asano, Seijro MATSUBARA Keisuke Asano, Seijro MATSUBARA Asymmetric Cycloetherification by Bifunctional Organocatalyst Asymmetric Cycloetherification by Bifunctional Organocatalyst Synthesis , 50, 4243-4253 Synthesis , 50, 4243-4253 , 50, 4243-4253 2018/09 Refereed English Disclose to all
松原 誠二郎 松原 誠二郎 Chematicaは有機合成に新たな道を拓くのか?—AIと化学の未来像を探る Chematicaは有機合成に新たな道を拓くのか?—AIと化学の未来像を探る 化学, 73, 6, 532-535 化学, 73, 6, 532-535 , 73, 6, 532-535 2018/06 Refereed Japanese Research paper(scientific journal) Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA Catalytic Approaches to Optically Active 1,5-Benzothiazepines Catalytic Approaches to Optically Active 1,5-Benzothiazepines ACS Catal., 8, 7, 6273-6282 ACS Catal., 8, 7, 6273-6282 , 8, 7, 6273-6282 2018/05 Refereed English Research paper(scientific journal) Disclose to all
Takuya Kurahashi, Seijiro MATSUBARA Takuya Kurahashi, Seijiro MATSUBARA Ligand-controlled Behavior of Ag(I)–π Complex as σ-Lewis Acid Ligand-controlled Behavior of Ag(I)–π Complex as σ-Lewis Acid Chem. Lett., 47, 532-535 Chem. Lett., 47, 532-535 , 47, 532-535 2018/04 Refereed English Research paper(scientific journal) Disclose to all
Seijiro MATSUBARA Seijiro MATSUBARA Molecular Transformations Using Bis(iodozincio)methane­–The Role of Chelation in Main Group Organometallic Chemistry Molecular Transformations Using Bis(iodozincio)methane­–The Role of Chelation in Main Group Organometallic Chemistry Bull. Chem. Soc. Jpn., 91, 82-86 Bull. Chem. Soc. Jpn., 91, 82-86 , 91, 82-86 2018/01 Refereed English Research paper(scientific journal) Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA Asymmetric Net Cycloaddition for Access to Diverse Substituted 1,5-Benzothiazepines Asymmetric Net Cycloaddition for Access to Diverse Substituted 1,5-Benzothiazepines J. Org. Chem., 82, 12655-12688 J. Org. Chem., 82, 12655-12688 , 82, 12655-12688 2017/11 Refereed English Research paper(scientific journal) Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA Organocatalytic Enantio- and Diastereoselective Cycloetherification via Dynamic Kinetic Resolution of Chiral Cyanohydrins Organocatalytic Enantio- and Diastereoselective Cycloetherification via Dynamic Kinetic Resolution of Chiral Cyanohydrins Nat. Commun., 8, 1397-1397 Nat. Commun., 8, 1397-1397 , 8, 1397-1397 2017/11 Refereed English Research paper(scientific journal) Disclose to all
松原 誠二郎 松原 誠二郎 反応溶液の中身を見ようとした話 ~有機反応における「均一溶液」について~ 反応溶液の中身を見ようとした話 ~有機反応における「均一溶液」について~ 化学と工業, 70, 1110-1112 化学と工業, 70, 1110-1112 , 70, 1110-1112 2017/11 Refereed Japanese Research paper(scientific journal) Disclose to all
Yukako Shimada, Seijiro MATSUBARA Yukako Shimada, Seijiro MATSUBARA Preparation of Organozinc Reagents via Catalyst Controlled Three-Component Coupling between Alkyne, Iodoarene, and Bis(iodozincio)methane Preparation of Organozinc Reagents via Catalyst Controlled Three-Component Coupling between Alkyne, Iodoarene, and Bis(iodozincio)methane Org. Lett., 19, 3335-3337 Org. Lett., 19, 3335-3337 , 19, 3335-3337 2017/06 Refereed English Research paper(scientific journal) Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA Bifunctional Organocatalysts for the Asymmetric Synthesis of Axially Chiral Benzamides Bifunctional Organocatalysts for the Asymmetric Synthesis of Axially Chiral Benzamides Beilstein J. Org. Chem., 13, 1518-1523 Beilstein J. Org. Chem., 13, 1518-1523 , 13, 1518-1523 2017/06 Refereed English Research paper(scientific journal) Disclose to all
Keisuke Asano, Seijiro MATSUBARA Keisuke Asano, Seijiro MATSUBARA Induction of Axial Chirality in 8-Arylquinolines via Halogenation Reactions Using Bifunctional Organocatalysts Induction of Axial Chirality in 8-Arylquinolines via Halogenation Reactions Using Bifunctional Organocatalysts , 23, 9996-10000 , 23, 9996-10000 , 23, 9996-10000 2017/04 Refereed English Research paper(scientific journal) Disclose to all
MATSUBARA Seijiro Keisuke Asano, Seijiro MATSUBARA MATSUBARA Seijiro Asymmetric Cycloetherification via the Kinetic Resolution of Alcohols Using Chiral Phosphoric Acid Catalysts Asymmetric Cycloetherification via the Kinetic Resolution of Alcohols Using Chiral Phosphoric Acid Catalysts Asymmetric Cycloetherification via the Kinetic Resolution of Alcohols Using Chiral Phosphoric Acid Catalysts Chem. Lett., 45, 11, 1300-1303 Chem. Lett., 45, 11, 1300-1303 , 45, 11, 1300-1303 2016/11 Refereed English Research paper(scientific journal) Disclose to all
Miyaji, R.; Asano, K.; Matsubara, S. Miyaji, R.; Asano, K.; Matsubara, S. Miyaji, R.; Asano, K.; Matsubara, S. Bifunctional Organocatalysts for the Enantioselective Synthesis of Axially Chiral Isoquinoline N-Oxides Bifunctional Organocatalysts for the Enantioselective Synthesis of Axially Chiral Isoquinoline N-Oxides Bifunctional Organocatalysts for the Enantioselective Synthesis of Axially Chiral Isoquinoline N-Oxides Journal of the American Chemical Society, 137, 21, 6766-6769 Journal of the American Chemical Society, 137, 21, 6766-6769 Journal of the American Chemical Society, 137, 21, 6766-6769 2015/05 Refereed English Research paper(scientific journal) Disclose to all
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro Organozinc Reagents in a Flow-microreactor -From Methylenation to Asymmetric Autocatalysis- Organozinc Reagents in a Flow-microreactor -From Methylenation to Asymmetric Autocatalysis- Organozinc Reagents in a Flow-microreactor -From Methylenation to Asymmetric Autocatalysis- JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 73, 5, 435-441 JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 73, 5, 435-441 JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 73, 5, 435-441 2015/05 Refereed Japanese Research paper(scientific journal) Disclose to all
Fukata, T.; Asano, K.; Matsubara, S. Fukata, T.; Asano, K.; Matsubara, S. Fukata, T.; Asano, K.; Matsubara, S. Facile Net Cycloaddition Approach to Optically Active 1,5-Benzothiazepines Facile Net Cycloaddition Approach to Optically Active 1,5-Benzothiazepines Facile Net Cycloaddition Approach to Optically Active 1,5-Benzothiazepines Journal of the American Chemical Society, 137, 16, 5320-5323 Journal of the American Chemical Society, 137, 16, 5320-5323 Journal of the American Chemical Society, 137, 16, 5320-5323 2015/04 Refereed English Research paper(scientific journal) Disclose to all
Inami, T.; Kurahashi, T.; Matsubara, S. Inami, T.; Kurahashi, T.; Matsubara, S. Inami, T.; Kurahashi, T.; Matsubara, S. Nickel-catalysed synthesis of tetrasubstituted vinyl sulfides from thiocarbamates and internal alkynes Nickel-catalysed synthesis of tetrasubstituted vinyl sulfides from thiocarbamates and internal alkynes Nickel-catalysed synthesis of tetrasubstituted vinyl sulfides from thiocarbamates and internal alkynes Chemical Communication, 51, 7, 1285-1288 Chemical Communication, 51, 7, 1285-1288 Chemical Communication, 51, 7, 1285-1288 2015/01 Refereed English Research paper(scientific journal) Disclose to all
Guan, W.; Sakaki, S.; Kurahashi, T.; Matsubara, S, Guan, W.; Sakaki, S.; Kurahashi, T.; Matsubara, S, Guan, W.; Sakaki, S.; Kurahashi, T.; Matsubara, S, Reasons Two Nonstrained C-C sigma-Bonds Can Be Easily Cleaved in Decyanative [4+2] Cycloaddition Catalyzed by Nickel(0)/Lewis Acid Systems. Theoretical Insight Reasons Two Nonstrained C-C sigma-Bonds Can Be Easily Cleaved in Decyanative [4+2] Cycloaddition Catalyzed by Nickel(0)/Lewis Acid Systems. Theoretical Insight Reasons Two Nonstrained C-C sigma-Bonds Can Be Easily Cleaved in Decyanative [4+2] Cycloaddition Catalyzed by Nickel(0)/Lewis Acid Systems. Theoretical Insight ACS Catalysis, 5, 1, 1-10 ACS Catalysis, 5, 1, 1-10 ACS Catalysis, 5, 1, 1-10 2015/01 Refereed English Research paper(scientific journal) Disclose to all
Ryosuke, H.; Takada, Y.; Matsubara, S. Ryosuke, H.; Takada, Y.; Matsubara, S. Ryosuke, H.; Takada, Y.; Matsubara, S. Preparation of cycloheptane ring by nucleophilic cyclopropanation of 1,2-diketones with bis(iodozincio)methane Preparation of cycloheptane ring by nucleophilic cyclopropanation of 1,2-diketones with bis(iodozincio)methane Preparation of cycloheptane ring by nucleophilic cyclopropanation of 1,2-diketones with bis(iodozincio)methane Organic & Biomolecular Chemistry, 13, 1, 241-247 Organic & Biomolecular Chemistry, 13, 1, 241-247 Organic & Biomolecular Chemistry, 13, 1, 241-247 2015/01 Refereed English Research paper(scientific journal) Disclose to all
Sada, M.; Uchiyama, M.; Matsubara, S. Sada, M.; Uchiyama, M.; Matsubara, S. Sada, M.; Uchiyama, M.; Matsubara, S. Design of Molecular Transformations Based on the Concerted Function of Two Zinc Atoms in Bis(iodozincio)methane Design of Molecular Transformations Based on the Concerted Function of Two Zinc Atoms in Bis(iodozincio)methane Design of Molecular Transformations Based on the Concerted Function of Two Zinc Atoms in Bis(iodozincio)methane Synlett, 25, 20, 2831-2841 Synlett, 25, 20, 2831-2841 Synlett, 25, 20, 2831-2841 2014/12 Refereed English Research paper(scientific journal) Disclose to all
Hasegawa, M.; Kurahashi, T.; Matsubara, S. Hasegawa, M.; Kurahashi, T.; Matsubara, S. Hasegawa, M.; Kurahashi, T.; Matsubara, S. Rhodium(III) Porphyrin-catalyzed Reactions via Activation of Alkynes Rhodium(III) Porphyrin-catalyzed Reactions via Activation of Alkynes Rhodium(III) Porphyrin-catalyzed Reactions via Activation of Alkynes Chemistry Letters, 43, 12, 1937-1939 Chemistry Letters, 43, 12, 1937-1939 Chemistry Letters, 43, 12, 1937-1939 2014/12 Refereed English Disclose to all
Yoneda, N.; Hotta, A.; Asano, K.; Matsubara, S. Yoneda, N.; Hotta, A.; Asano, K.; Matsubara, S. Yoneda, N.; Hotta, A.; Asano, K.; Matsubara, S. Asymmetric Oxy-Michael Addition to γ-Hydroxy-α,β-Unsaturated Carbonyls Using Formaldehyde as an Oxygen-Centered Nucleophile Asymmetric Oxy-Michael Addition to γ-Hydroxy-α,β-Unsaturated Carbonyls Using Formaldehyde as an Oxygen-Centered Nucleophile Asymmetric Oxy-Michael Addition to γ-Hydroxy-α,β-Unsaturated Carbonyls Using Formaldehyde as an Oxygen-Centered Nucleophile Organic Letters, 16, 23, 6264-6266 Organic Letters, 16, 23, 6264-6266 Organic Letters, 16, 23, 6264-6266 2014/12 Refereed English Research paper(scientific journal) Disclose to all
Inami, T.; Kurahashi, T.; Matsubara, S. Inami, T.; Kurahashi, T.; Matsubara, S. Inami, T.; Kurahashi, T.; Matsubara, S. Nickel-Catalyzed Reaction of Thioisatins and Alkynes: A Facile Synthesis of Thiochromones Nickel-Catalyzed Reaction of Thioisatins and Alkynes: A Facile Synthesis of Thiochromones Nickel-Catalyzed Reaction of Thioisatins and Alkynes: A Facile Synthesis of Thiochromones Organic Letters, 16, 21, 5660-5662 Organic Letters, 16, 21, 5660-5662 Organic Letters, 16, 21, 5660-5662 2014/11 Refereed English Research paper(scientific journal) Disclose to all
Tombe, R.; Iwamoto, T.; Kurahashi, T.; Matsubara, S. Tombe, R.; Iwamoto, T.; Kurahashi, T.; Matsubara, S. Tombe, R.; Iwamoto, T.; Kurahashi, T.; Matsubara, S. Regio- and Diastereoselective Nickel-Catalyzed Cycloaddition of Activated Cyclopropanes with Allenes Regio- and Diastereoselective Nickel-Catalyzed Cycloaddition of Activated Cyclopropanes with Allenes Regio- and Diastereoselective Nickel-Catalyzed Cycloaddition of Activated Cyclopropanes with Allenes Synlett, 25, 16, 2281-2284 Synlett, 25, 16, 2281-2284 Synlett, 25, 16, 2281-2284 2014/10 Refereed English Research paper(scientific journal) Disclose to all
Haraguchi, R.; Matsubara, S. Haraguchi, R.; Matsubara, S. Haraguchi, R.; Matsubara, S. Preparation of the Zinc Enolate Equivalent of Amides by Zinciomethylation of Isocyanates: Catalytic Asymmetric Reformatsky-Type Reaction Preparation of the Zinc Enolate Equivalent of Amides by Zinciomethylation of Isocyanates: Catalytic Asymmetric Reformatsky-Type Reaction Preparation of the Zinc Enolate Equivalent of Amides by Zinciomethylation of Isocyanates: Catalytic Asymmetric Reformatsky-Type Reaction Synthesis, 46, 17, 2272-2282 Synthesis, 46, 17, 2272-2282 Synthesis, 46, 17, 2272-2282 2014/09 Refereed English Research paper(scientific journal) Disclose to all
Sai,M.; Matsubara, S. Sai,M.; Matsubara, S. Sai,M.; Matsubara, S. Lithium(1+)-Catalyzed Nazarov-Type Cyclization of 1-Arylbuta-2,3-dien-1-ols: Synthesis of Benzofulvene Derivatives Lithium(1+)-Catalyzed Nazarov-Type Cyclization of 1-Arylbuta-2,3-dien-1-ols: Synthesis of Benzofulvene Derivatives Lithium(1+)-Catalyzed Nazarov-Type Cyclization of 1-Arylbuta-2,3-dien-1-ols: Synthesis of Benzofulvene Derivatives Synlett, 25, 14, 2067-2071 Synlett, 25, 14, 2067-2071 Synlett, 25, 14, 2067-2071 2014/09 Refereed English Research paper(scientific journal) Disclose to all
Shiba, Takahiro; Kuroda, Daiki; Kurahashi, T.; Matsubara, S. Shiba, Takahiro; Kuroda, Daiki; Kurahashi, T.; Matsubara, S. Shiba, Takahiro; Kuroda, Daiki; Kurahashi, T.; Matsubara, S. Cobalt Porphyrin Catalyzed [3+2] Cycloaddition of Cyclopropanes and Carbonyl Compounds Cobalt Porphyrin Catalyzed [3+2] Cycloaddition of Cyclopropanes and Carbonyl Compounds Cobalt Porphyrin Catalyzed [3+2] Cycloaddition of Cyclopropanes and Carbonyl Compounds Synlett, 25, 14, 2005-2008 Synlett, 25, 14, 2005-2008 Synlett, 25, 14, 2005-2008 2014/09 Refereed English Research paper(scientific journal) Disclose to all
Nishibayashi, R.; Kurahashi, T.; Matsubara, S. Nishibayashi, R.; Kurahashi, T.; Matsubara, S. Nishibayashi, R.; Kurahashi, T.; Matsubara, S. Palladium Porphyrin Catalyzed Hydrogenation of Alkynes: Stereoselective Synthesis of cis-Alkenes Palladium Porphyrin Catalyzed Hydrogenation of Alkynes: Stereoselective Synthesis of cis-Alkenes Palladium Porphyrin Catalyzed Hydrogenation of Alkynes: Stereoselective Synthesis of cis-Alkenes Synlett, 25, 9, 1287-1290 Synlett, 25, 9, 1287-1290 Synlett, 25, 9, 1287-1290 2014/06 Refereed English Research paper(scientific journal) Disclose to all
Nakai, K.; Yoshida, Y.; Kurahashi, T.; Matsubara, S. Nakai, K.; Yoshida, Y.; Kurahashi, T.; Matsubara, S. Nakai, K.; Yoshida, Y.; Kurahashi, T.; Matsubara, S. Nickel-Catalyzed Redox-Economical Coupling of Alcohols and Alkynes to Form Allylic Alcohols Nickel-Catalyzed Redox-Economical Coupling of Alcohols and Alkynes to Form Allylic Alcohols Nickel-Catalyzed Redox-Economical Coupling of Alcohols and Alkynes to Form Allylic Alcohols Journal of the American Chemical Society, 136, 22, 7797-7800 Journal of the American Chemical Society, 136, 22, 7797-7800 Journal of the American Chemical Society, 136, 22, 7797-7800 2014/06 Refereed English Research paper(scientific journal) Disclose to all
Terada, T.; Kurahashi, T.; Matsubara, S. Terada, T.; Kurahashi, T.; Matsubara, S. Terada, T.; Kurahashi, T.; Matsubara, S. Diastereoselective Construction of Trans-Fused Octalone Framework via Ruthenium-Porphyrin-Catalyzed Cycloaddition Diastereoselective Construction of Trans-Fused Octalone Framework via Ruthenium-Porphyrin-Catalyzed Cycloaddition Diastereoselective Construction of Trans-Fused Octalone Framework via Ruthenium-Porphyrin-Catalyzed Cycloaddition Organic Letters, 16, 10, 2594-2597 Organic Letters, 16, 10, 2594-2597 Organic Letters, 16, 10, 2594-2597 2014/05 Refereed English Research paper(scientific journal) Disclose to all
Fukata, Y.; Okamura, T.; Asano, K.; Matsubara, S. Fukata, Y.; Okamura, T.; Asano, K.; Matsubara, S. Fukata, Y.; Okamura, T.; Asano, K.; Matsubara, S. Asymmetric Isomerization of ω-Hydroxy-α,β-Unsaturated Thioesters into β -Mercaptolactones by a Bifunctional Aminothiourea Catalyst Asymmetric Isomerization of ω-Hydroxy-α,β-Unsaturated Thioesters into β -Mercaptolactones by a Bifunctional Aminothiourea Catalyst Asymmetric Isomerization of ω-Hydroxy-α,β-Unsaturated Thioesters into β -Mercaptolactones by a Bifunctional Aminothiourea Catalyst Organic Letters, 16, 8, 2184-2187 Organic Letters, 16, 8, 2184-2187 Organic Letters, 16, 8, 2184-2187 2014/04 Refereed English Research paper(scientific journal) Disclose to all
R. Miyaji; K. Asano; S. Matsubara R. Miyaji; K. Asano; S. Matsubara R. Miyaji; K. Asano; S. Matsubara Asymmetric chroman synthesis via an intramolecular oxy-Michael addition by bifunctional organocatalysts Asymmetric chroman synthesis via an intramolecular oxy-Michael addition by bifunctional organocatalysts Asymmetric chroman synthesis via an intramolecular oxy-Michael addition by bifunctional organocatalysts Organic and Biomolecular Chemistry, 12, 1, 119-122 Organic and Biomolecular Chemistry, 12, 1, 119-122 Organic and Biomolecular Chemistry, 12, 1, 119-122 2014/01/07 Refereed English Disclose to all
Y. Fukata; K. Asano; S. Matsubara Y. Fukata; K. Asano; S. Matsubara Y. Fukata; K. Asano; S. Matsubara Procedure-controlled enantioselectivity switch in organocatalytic 2-oxazolidinone synthesis Procedure-controlled enantioselectivity switch in organocatalytic 2-oxazolidinone synthesis Procedure-controlled enantioselectivity switch in organocatalytic 2-oxazolidinone synthesis Journal of the American Chemical Society, 135, 33, 12160-12163 Journal of the American Chemical Society, 135, 33, 12160-12163 Journal of the American Chemical Society, 135, 33, 12160-12163 2013/08/21 Refereed English Disclose to all
R. Miyaji; K. Asano; S. Matsubara R. Miyaji; K. Asano; S. Matsubara R. Miyaji; K. Asano; S. Matsubara Asymmetric indoline synthesis via intramolecular aza-Michael addition mediated by bifunctional organocatalysts Asymmetric indoline synthesis via intramolecular aza-Michael addition mediated by bifunctional organocatalysts Asymmetric indoline synthesis via intramolecular aza-Michael addition mediated by bifunctional organocatalysts Organic Letters, 15, 14, 3658-3661 Organic Letters, 15, 14, 3658-3661 Organic Letters, 15, 14, 3658-3661 2013/07/19 Refereed English Disclose to all
Y. Fukata; R. Miyaji; T. Okamura; K. Asano; S. Matsubara Y. Fukata; R. Miyaji; T. Okamura; K. Asano; S. Matsubara Y. Fukata; R. Miyaji; T. Okamura; K. Asano; S. Matsubara Asymmetric cycloetherifications by bifunctional aminothiourea catalysts: The importance of hydrogen bonding Asymmetric cycloetherifications by bifunctional aminothiourea catalysts: The importance of hydrogen bonding Asymmetric cycloetherifications by bifunctional aminothiourea catalysts: The importance of hydrogen bonding Synthesis (Germany), 45, 12, 1627-1634 Synthesis (Germany), 45, 12, 1627-1634 Synthesis (Germany), 45, 12, 1627-1634 2013/06 Refereed English Disclose to all
Y. Fukata; K. Asano; S. Matsubara Y. Fukata; K. Asano; S. Matsubara Y. Fukata; K. Asano; S. Matsubara Asymmetric synthesis of 1,3-oxazolidines via intramolecular aza-michael addition by bifunctional organocatalysts Asymmetric synthesis of 1,3-oxazolidines via intramolecular aza-michael addition by bifunctional organocatalysts Asymmetric synthesis of 1,3-oxazolidines via intramolecular aza-michael addition by bifunctional organocatalysts Chemistry Letters, 42, 4, 355-357 Chemistry Letters, 42, 4, 355-357 Chemistry Letters, 42, 4, 355-357 2013/04/05 Refereed English Disclose to all
K. Nakai; T. Kurahashi; S. Matsubara K. Nakai; T. Kurahashi; S. Matsubara K. Nakai; T. Kurahashi; S. Matsubara Synthesis of quinolones by nickel-catalyzed cycloaddition via elimination of nitrile Synthesis of quinolones by nickel-catalyzed cycloaddition via elimination of nitrile Synthesis of quinolones by nickel-catalyzed cycloaddition via elimination of nitrile Organic Letters, 15, 4, 856-859 Organic Letters, 15, 4, 856-859 Organic Letters, 15, 4, 856-859 2013 Refereed English Disclose to all
R. Tombe; T. Kurahashi; S. Matsubara R. Tombe; T. Kurahashi; S. Matsubara R. Tombe; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of vinylcyclopropanes to imines Nickel-catalyzed cycloaddition of vinylcyclopropanes to imines Nickel-catalyzed cycloaddition of vinylcyclopropanes to imines Organic Letters, 15, 8, 1791-1793 Organic Letters, 15, 8, 1791-1793 Organic Letters, 15, 8, 1791-1793 2013 Refereed English Disclose to all
H. Katayama; S. Matsubara H. Katayama; S. Matsubara H. Katayama; S. Matsubara Copper-catalyzed 1,4-addition reaction of Grignard reagent to enones using microflow system Copper-catalyzed 1,4-addition reaction of Grignard reagent to enones using microflow system Copper-catalyzed 1,4-addition reaction of Grignard reagent to enones using microflow system Chemistry Letters, 42, 5, 471-472 Chemistry Letters, 42, 5, 471-472 Chemistry Letters, 42, 5, 471-472 2013 Refereed English Disclose to all
R. Haraguchi; S. Matsubara R. Haraguchi; S. Matsubara R. Haraguchi; S. Matsubara Catalytic asymmetric aldol-type reaction of zinc enolate equivalent of amides Catalytic asymmetric aldol-type reaction of zinc enolate equivalent of amides Catalytic asymmetric aldol-type reaction of zinc enolate equivalent of amides Organic Letters, 15, 13, 3378-3380 Organic Letters, 15, 13, 3378-3380 Organic Letters, 15, 13, 3378-3380 2013 Refereed English Disclose to all
S. Teranishi; T. Kurahashi; S. Matsubara S. Teranishi; T. Kurahashi; S. Matsubara S. Teranishi; T. Kurahashi; S. Matsubara Cationic Iron(III) porphyrin catalyzed dehydrative friedel-crafts reaction of alcohols with arenes Cationic Iron(III) porphyrin catalyzed dehydrative friedel-crafts reaction of alcohols with arenes Cationic Iron(III) porphyrin catalyzed dehydrative friedel-crafts reaction of alcohols with arenes Synlett, 24, 16, 2148-2152 Synlett, 24, 16, 2148-2152 Synlett, 24, 16, 2148-2152 2013 Refereed English Disclose to all
R. Wakabayashi; T. Kurahashi; S. Matsubara R. Wakabayashi; T. Kurahashi; S. Matsubara R. Wakabayashi; T. Kurahashi; S. Matsubara Synthesis of phenanthrenes by cationic chromium(III) porphyrin-catalyzed dehydration cycloaromatization Synthesis of phenanthrenes by cationic chromium(III) porphyrin-catalyzed dehydration cycloaromatization Synthesis of phenanthrenes by cationic chromium(III) porphyrin-catalyzed dehydration cycloaromatization Synlett, 24, 17, 2297-2301 Synlett, 24, 17, 2297-2301 Synlett, 24, 17, 2297-2301 2013 Refereed English Disclose to all
T. Shiba; T. Kurahashi; S. Matsubara T. Shiba; T. Kurahashi; S. Matsubara T. Shiba; T. Kurahashi; S. Matsubara Nickel-catalyzed decarbonylative alkylidenation of phthalimides with trimethylsilyl-substituted alkynes Nickel-catalyzed decarbonylative alkylidenation of phthalimides with trimethylsilyl-substituted alkynes Nickel-catalyzed decarbonylative alkylidenation of phthalimides with trimethylsilyl-substituted alkynes Journal of the American Chemical Society, 135, 37, 13636-13639 Journal of the American Chemical Society, 135, 37, 13636-13639 Journal of the American Chemical Society, 135, 37, 13636-13639 2013 Refereed English Disclose to all
K. Nakai; T. Kurahashi; S. Matsubara K. Nakai; T. Kurahashi; S. Matsubara K. Nakai; T. Kurahashi; S. Matsubara Nickel-catalyzed decarbonylative and decarboxylative cycloaddition of isatoic anhydrides with alkynes Nickel-catalyzed decarbonylative and decarboxylative cycloaddition of isatoic anhydrides with alkynes Nickel-catalyzed decarbonylative and decarboxylative cycloaddition of isatoic anhydrides with alkynes Chemistry Letters, 42, 10, 1238-1240 Chemistry Letters, 42, 10, 1238-1240 Chemistry Letters, 42, 10, 1238-1240 2013 Refereed English Disclose to all
T. Kuwano; T. Kurahashi; S. Matsubara T. Kuwano; T. Kurahashi; S. Matsubara T. Kuwano; T. Kurahashi; S. Matsubara Iron corrole-catalyzed [4 + 2] cycloaddition of dienes and aldehydes Iron corrole-catalyzed [4 + 2] cycloaddition of dienes and aldehydes Iron corrole-catalyzed [4 + 2] cycloaddition of dienes and aldehydes Chemistry Letters, 42, 10, 1241-1243 Chemistry Letters, 42, 10, 1241-1243 Chemistry Letters, 42, 10, 1241-1243 2013 Refereed English Disclose to all
M. Hasegawa; T. Kurahashi; S. Matsubara M. Hasegawa; T. Kurahashi; S. Matsubara M. Hasegawa; T. Kurahashi; S. Matsubara Dicationic platinum porphyrin catalyzed cycloisomerization of enynes Dicationic platinum porphyrin catalyzed cycloisomerization of enynes Dicationic platinum porphyrin catalyzed cycloisomerization of enynes Tetrahedron Letters, 54, 46, 6196-6198 Tetrahedron Letters, 54, 46, 6196-6198 Tetrahedron Letters, 54, 46, 6196-6198 2013 Refereed English Disclose to all
T. Ozawa; T. Kurahashi; S. Matsubara T. Ozawa; T. Kurahashi; S. Matsubara T. Ozawa; T. Kurahashi; S. Matsubara L[e3tte+r 2] cycloaddition of aziridines and alkenes catalyzed by a cationic manganese porphyrin L[e3tte+r 2] cycloaddition of aziridines and alkenes catalyzed by a cationic manganese porphyrin L[e3tte+r 2] cycloaddition of aziridines and alkenes catalyzed by a cationic manganese porphyrin Synlett, 24, 20, 2763-2767 Synlett, 24, 20, 2763-2767 Synlett, 24, 20, 2763-2767 2013 Refereed English Disclose to all
W. Guan; S. Sakaki; T. Kurahashi; S. Matsubara W. Guan; S. Sakaki; T. Kurahashi; S. Matsubara W. Guan; S. Sakaki; T. Kurahashi; S. Matsubara Theoretical mechanistic study of novel Ni(0)-catalyzed [6 - 2 + 2] cycloaddition reactions of isatoic anhydrides with alkynes: Origin of facile decarboxylation Theoretical mechanistic study of novel Ni(0)-catalyzed [6 - 2 + 2] cycloaddition reactions of isatoic anhydrides with alkynes: Origin of facile decarboxylation Theoretical mechanistic study of novel Ni(0)-catalyzed [6 - 2 + 2] cycloaddition reactions of isatoic anhydrides with alkynes: Origin of facile decarboxylation Organometallics, 32, 24, 7564-7574 Organometallics, 32, 24, 7564-7574 Organometallics, 32, 24, 7564-7574 2013 Refereed English Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara Asymmetric synthesis of 1,3-dioxolanes by organocatalytic formal [3 + 2] cycloaddition via hemiacetal intermediates Asymmetric synthesis of 1,3-dioxolanes by organocatalytic formal [3 + 2] cycloaddition via hemiacetal intermediates Asymmetric synthesis of 1,3-dioxolanes by organocatalytic formal [3 + 2] cycloaddition via hemiacetal intermediates Organic Letters, 14, 6, 1620-1623 Organic Letters, 14, 6, 1620-1623 Organic Letters, 14, 6, 1620-1623 2012/03/16 Refereed English Disclose to all
R. Tombe; S. Matsubara R. Tombe; S. Matsubara R. Tombe; S. Matsubara Preparation of furan ring from 2-(Oxiran-2-YL)-1-Alkylethanone catalyzed by nafion® SAC-13 Preparation of furan ring from 2-(Oxiran-2-YL)-1-Alkylethanone catalyzed by nafion® SAC-13 Preparation of furan ring from 2-(Oxiran-2-YL)-1-Alkylethanone catalyzed by nafion® SAC-13 Heterocycles, 84, 2, 775-783 Heterocycles, 84, 2, 775-783 Heterocycles, 84, 2, 775-783 2012 Refereed English Disclose to all
H. Horie; T. Kurahashi; S. Matsubara H. Horie; T. Kurahashi; S. Matsubara H. Horie; T. Kurahashi; S. Matsubara Nickel-catalyzed [4+2] cycloaddition for highly substituted arenes Nickel-catalyzed [4+2] cycloaddition for highly substituted arenes Nickel-catalyzed [4+2] cycloaddition for highly substituted arenes Chemical Communications, 48, 32, 3866-3868 Chemical Communications, 48, 32, 3866-3868 Chemical Communications, 48, 32, 3866-3868 2012 Refereed English Disclose to all
K. Fujiwara; T. Kurahashi; S. Matsubara K. Fujiwara; T. Kurahashi; S. Matsubara K. Fujiwara; T. Kurahashi; S. Matsubara Cationic iron(III) porphyrin-catalyzed [4 + 2] cycloaddition of unactivated aldehydes with simple dienes Cationic iron(III) porphyrin-catalyzed [4 + 2] cycloaddition of unactivated aldehydes with simple dienes Cationic iron(III) porphyrin-catalyzed [4 + 2] cycloaddition of unactivated aldehydes with simple dienes Journal of the American Chemical Society, 134, 12, 5512-5515 Journal of the American Chemical Society, 134, 12, 5512-5515 Journal of the American Chemical Society, 134, 12, 5512-5515 2012 Refereed English Disclose to all
T. Okamura; K. Asano; S. Matsubara T. Okamura; K. Asano; S. Matsubara T. Okamura; K. Asano; S. Matsubara Organocatalytic asymmetric oxy-Michael addition to a γ-hydroxy- α,β-unsaturated thioester via hemiacetal intermediates Organocatalytic asymmetric oxy-Michael addition to a γ-hydroxy- α,β-unsaturated thioester via hemiacetal intermediates Organocatalytic asymmetric oxy-Michael addition to a γ-hydroxy- α,β-unsaturated thioester via hemiacetal intermediates Chemical Communications, 48, 42, 5076-5078 Chemical Communications, 48, 42, 5076-5078 Chemical Communications, 48, 42, 5076-5078 2012 Refereed English Disclose to all
R. Haraguchi; Y. Takada; S. Matsubara R. Haraguchi; Y. Takada; S. Matsubara R. Haraguchi; Y. Takada; S. Matsubara Rapid preparation of cycloheptane ring from 1,2-diketone and bis(iodozincio)methane via oxy-cope rearrangement using microflow system Rapid preparation of cycloheptane ring from 1,2-diketone and bis(iodozincio)methane via oxy-cope rearrangement using microflow system Rapid preparation of cycloheptane ring from 1,2-diketone and bis(iodozincio)methane via oxy-cope rearrangement using microflow system Chemistry Letters, 41, 6, 628-629 Chemistry Letters, 41, 6, 628-629 Chemistry Letters, 41, 6, 628-629 2012 Refereed English Disclose to all
T. Ozawa; T. Kurahashi; S. Matsubara T. Ozawa; T. Kurahashi; S. Matsubara T. Ozawa; T. Kurahashi; S. Matsubara Manganese porphyrin catalyzed cycloisomerization of enynes Manganese porphyrin catalyzed cycloisomerization of enynes Manganese porphyrin catalyzed cycloisomerization of enynes Organic Letters, 14, 12, 3008-3011 Organic Letters, 14, 12, 3008-3011 Organic Letters, 14, 12, 3008-3011 2012 Refereed English Disclose to all
T. Terada; T. Kurahashi; S. Matsubara T. Terada; T. Kurahashi; S. Matsubara T. Terada; T. Kurahashi; S. Matsubara Ruthenium porphyrin catalyzed friedel-crafts type reaction of arenes with imines Ruthenium porphyrin catalyzed friedel-crafts type reaction of arenes with imines Ruthenium porphyrin catalyzed friedel-crafts type reaction of arenes with imines Heterocycles, 85, 10, 2415-2419 Heterocycles, 85, 10, 2415-2419 Heterocycles, 85, 10, 2415-2419 2012 Refereed English Disclose to all
R. Wakabayashi; T. Kurahashi; S. Matsubara R. Wakabayashi; T. Kurahashi; S. Matsubara R. Wakabayashi; T. Kurahashi; S. Matsubara Cobalt(III) porphyrin catalyzed aza-Diels-Alder reaction Cobalt(III) porphyrin catalyzed aza-Diels-Alder reaction Cobalt(III) porphyrin catalyzed aza-Diels-Alder reaction Organic Letters, 14, 18, 4794-4797 Organic Letters, 14, 18, 4794-4797 Organic Letters, 14, 18, 4794-4797 2012 Refereed English Disclose to all
M. Takeuchi; T. Kurahashi; S. Matsubara M. Takeuchi; T. Kurahashi; S. Matsubara M. Takeuchi; T. Kurahashi; S. Matsubara Nickel-catalyzed decarbonylative polymerization of 5-alkynylphthalimides: A new methodology for the preparation of polyheterocycles Nickel-catalyzed decarbonylative polymerization of 5-alkynylphthalimides: A new methodology for the preparation of polyheterocycles Nickel-catalyzed decarbonylative polymerization of 5-alkynylphthalimides: A new methodology for the preparation of polyheterocycles Chemistry Letters, 41, 12, 1566-1568 Chemistry Letters, 41, 12, 1566-1568 Chemistry Letters, 41, 12, 1566-1568 2012 Refereed English Disclose to all
Y. Yoshida; T. Kurahashi; S. Matsubara Y. Yoshida; T. Kurahashi; S. Matsubara Y. Yoshida; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of α,β-unsaturated oximes with alkynes: Synthesis of highly substituted pyridine derivatives Nickel-catalyzed cycloaddition of α,β-unsaturated oximes with alkynes: Synthesis of highly substituted pyridine derivatives Nickel-catalyzed cycloaddition of α,β-unsaturated oximes with alkynes: Synthesis of highly substituted pyridine derivatives Chemistry Letters, 41, 11, 1498-1499 Chemistry Letters, 41, 11, 1498-1499 Chemistry Letters, 41, 11, 1498-1499 2012 Refereed English Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara Asymmetric catalytic cycloetherification mediated by bifunctional organocatalysts Asymmetric catalytic cycloetherification mediated by bifunctional organocatalysts Asymmetric catalytic cycloetherification mediated by bifunctional organocatalysts Journal of the American Chemical Society, 133, 42, 16711-16713 Journal of the American Chemical Society, 133, 42, 16711-16713 Journal of the American Chemical Society, 133, 42, 16711-16713 2011/10/26 Refereed English Disclose to all
Ito, S.; Nishi, M.; Kanamori, K.; Nakanishi, K.; Kurahashi, T.; Matsubara, S.; Shimotsuma, Yasuhiko; Miura, Kiyotaka; Hirao, K. Ito, S.; Nishi, M.; Kanamori, K.; Nakanishi, K.; Kurahashi, T.; Matsubara, S.; Shimotsuma, Yasuhiko; Miura, Kiyotaka; Hirao, K. Ito, S.; Nishi, M.; Kanamori, K.; Nakanishi, K.; Kurahashi, T.; Matsubara, S.; Shimotsuma, Yasuhiko; Miura, Kiyotaka; Hirao, K. (3-Mercaptopropyl)trimethoxysilane-derived Porous Gel Monolith via Thioacetal Reaction-Assisted Sol-Gel Route (3-Mercaptopropyl)trimethoxysilane-derived Porous Gel Monolith via Thioacetal Reaction-Assisted Sol-Gel Route (3-Mercaptopropyl)trimethoxysilane-derived Porous Gel Monolith via Thioacetal Reaction-Assisted Sol-Gel Route 3RD INTERNATIONAL CONGRESS ON CERAMICS (ICC): NOVEL CHEMICAL PROCESSING SOL-GEL AND SOLUTION-BASED PROCESSING,18 (3), p. 032003 3RD INTERNATIONAL CONGRESS ON CERAMICS (ICC): NOVEL CHEMICAL PROCESSING SOL-GEL AND SOLUTION-BASED PROCESSING,18 (3), p. 032003 3RD INTERNATIONAL CONGRESS ON CERAMICS (ICC): NOVEL CHEMICAL PROCESSING SOL-GEL AND SOLUTION-BASED PROCESSING,18 (3), p. 032003 2011/10 Refereed English Disclose to all
M. Sada; K. Nomura; S. Matsubara M. Sada; K. Nomura; S. Matsubara M. Sada; K. Nomura; S. Matsubara A tandem reaction of organozinc reagent prepared from palladium-catalyzed umpolung method: Diastereoselective formation of cyclohexene derivatives bearing three adjacent stereocenters A tandem reaction of organozinc reagent prepared from palladium-catalyzed umpolung method: Diastereoselective formation of cyclohexene derivatives bearing three adjacent stereocenters A tandem reaction of organozinc reagent prepared from palladium-catalyzed umpolung method: Diastereoselective formation of cyclohexene derivatives bearing three adjacent stereocenters Organic and Biomolecular Chemistry, 9, 5, 1389-1393 Organic and Biomolecular Chemistry, 9, 5, 1389-1393 Organic and Biomolecular Chemistry, 9, 5, 1389-1393 2011 Refereed English Disclose to all
K. Fujiwara; T. Kurahashi; S. Matsubara K. Fujiwara; T. Kurahashi; S. Matsubara K. Fujiwara; T. Kurahashi; S. Matsubara Nickel-catalyzed decarbonylative cycloaddition of phthalic anhydrides with 1,3-Dienes Nickel-catalyzed decarbonylative cycloaddition of phthalic anhydrides with 1,3-Dienes Nickel-catalyzed decarbonylative cycloaddition of phthalic anhydrides with 1,3-Dienes Chemistry Letters, 40, 3, 322-323 Chemistry Letters, 40, 3, 322-323 Chemistry Letters, 40, 3, 322-323 2011 Refereed English Disclose to all
N. Maizuru; T. Inami; T. Kurahashi; S. Matsubara N. Maizuru; T. Inami; T. Kurahashi; S. Matsubara N. Maizuru; T. Inami; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of anthranilic acid derivatives to alkynes Nickel-catalyzed cycloaddition of anthranilic acid derivatives to alkynes Nickel-catalyzed cycloaddition of anthranilic acid derivatives to alkynes Organic Letters, 13, 5, 1206-1209 Organic Letters, 13, 5, 1206-1209 Organic Letters, 13, 5, 1206-1209 2011 Refereed English Disclose to all
H. Horie; I. Koyama; T. Kurahashi; S. Matsubara H. Horie; I. Koyama; T. Kurahashi; S. Matsubara H. Horie; I. Koyama; T. Kurahashi; S. Matsubara Nickel-catalyzed intermolecular codimerization of acrylates and alkynes Nickel-catalyzed intermolecular codimerization of acrylates and alkynes Nickel-catalyzed intermolecular codimerization of acrylates and alkynes Chemical Communications, 47, 9, 2658-2660 Chemical Communications, 47, 9, 2658-2660 Chemical Communications, 47, 9, 2658-2660 2011 Refereed English Disclose to all
M. Sada; S. Matsubara M. Sada; S. Matsubara M. Sada; S. Matsubara Transition-metal chloride mediated addition reaction of diorganomagnesium to easily enolizable ketones Transition-metal chloride mediated addition reaction of diorganomagnesium to easily enolizable ketones Transition-metal chloride mediated addition reaction of diorganomagnesium to easily enolizable ketones Tetrahedron, 67, 14, 2612-2616 Tetrahedron, 67, 14, 2612-2616 Tetrahedron, 67, 14, 2612-2616 2011 Refereed English Disclose to all
Y. Ochi; T. Kurahashi; S. Matsubara Y. Ochi; T. Kurahashi; S. Matsubara Y. Ochi; T. Kurahashi; S. Matsubara Decarbonylative cycloaddition of phthalic anhydrides with allenes Decarbonylative cycloaddition of phthalic anhydrides with allenes Decarbonylative cycloaddition of phthalic anhydrides with allenes Organic Letters, 13, 6, 1374-1377 Organic Letters, 13, 6, 1374-1377 Organic Letters, 13, 6, 1374-1377 2011 Refereed English Disclose to all
N. Maizuru; T. Inami; T. Kurahashi; S. Matsubara N. Maizuru; T. Inami; T. Kurahashi; S. Matsubara N. Maizuru; T. Inami; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloadditions of benzoxazinones with alkynes: Synthesis of quinolines and quinolones Nickel-catalyzed cycloadditions of benzoxazinones with alkynes: Synthesis of quinolines and quinolones Nickel-catalyzed cycloadditions of benzoxazinones with alkynes: Synthesis of quinolines and quinolones Chemistry Letters, 40, 4, 375-377 Chemistry Letters, 40, 4, 375-377 Chemistry Letters, 40, 4, 375-377 2011 Refereed English Disclose to all
Y. Takada; S. Matsubara Y. Takada; S. Matsubara Y. Takada; S. Matsubara Wittig like methylenation of aldehydes in a microflow system: Selective methylenation by differential of plural reactions Wittig like methylenation of aldehydes in a microflow system: Selective methylenation by differential of plural reactions Wittig like methylenation of aldehydes in a microflow system: Selective methylenation by differential of plural reactions Chemistry Letters, 40, 4, 364-365 Chemistry Letters, 40, 4, 364-365 Chemistry Letters, 40, 4, 364-365 2011 Refereed English Disclose to all
T. Inami; Y. Baba; T. Kurahashi; S. Matsubara T. Inami; Y. Baba; T. Kurahashi; S. Matsubara T. Inami; Y. Baba; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloadditions of thiophthalic anhydrideswith alkynes Nickel-catalyzed cycloadditions of thiophthalic anhydrideswith alkynes Nickel-catalyzed cycloadditions of thiophthalic anhydrideswith alkynes Organic Letters, 13, 8, 1912-1915 Organic Letters, 13, 8, 1912-1915 Organic Letters, 13, 8, 1912-1915 2011 Refereed English Disclose to all
S. Sako; T. Kurahashi; S. Matsubara S. Sako; T. Kurahashi; S. Matsubara S. Sako; T. Kurahashi; S. Matsubara Nickel-iminophosphine-catalyzed [4+2] cycloaddition of enones with allenes: Synthesis of highly substituted dihydropyrans Nickel-iminophosphine-catalyzed [4+2] cycloaddition of enones with allenes: Synthesis of highly substituted dihydropyrans Nickel-iminophosphine-catalyzed [4+2] cycloaddition of enones with allenes: Synthesis of highly substituted dihydropyrans Chemical Communications, 47, 21, 6150-6152 Chemical Communications, 47, 21, 6150-6152 Chemical Communications, 47, 21, 6150-6152 2011 Refereed English Disclose to all
S. Sako; T. Kurahashi; S. Matsubara S. Sako; T. Kurahashi; S. Matsubara S. Sako; T. Kurahashi; S. Matsubara Nickel-catalyzed [3 + 2] cycloaddition of α,β-unsaturated ketones with vinyl oxiranes Nickel-catalyzed [3 + 2] cycloaddition of α,β-unsaturated ketones with vinyl oxiranes Nickel-catalyzed [3 + 2] cycloaddition of α,β-unsaturated ketones with vinyl oxiranes Chemistry Letters, 40, 8, 808-809 Chemistry Letters, 40, 8, 808-809 Chemistry Letters, 40, 8, 808-809 2011 Refereed English Disclose to all
K. Nakai; T. Kurahashi; S. Matsubara K. Nakai; T. Kurahashi; S. Matsubara K. Nakai; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of o -arylcarboxybenzonitriles and alkynes via cleavage of two carbon - Carbon σ bonds Nickel-catalyzed cycloaddition of o -arylcarboxybenzonitriles and alkynes via cleavage of two carbon - Carbon σ bonds Nickel-catalyzed cycloaddition of o -arylcarboxybenzonitriles and alkynes via cleavage of two carbon - Carbon σ bonds Journal of the American Chemical Society, 133, 29, 11066-11068 Journal of the American Chemical Society, 133, 29, 11066-11068 Journal of the American Chemical Society, 133, 29, 11066-11068 2011 Refereed English Disclose to all
T. Inami; S. Sako; T. Kurahashi; S. Matsubara T. Inami; S. Sako; T. Kurahashi; S. Matsubara T. Inami; S. Sako; T. Kurahashi; S. Matsubara Methylenecyclopropanes in [4+1] cycloaddition with enones Methylenecyclopropanes in [4+1] cycloaddition with enones Methylenecyclopropanes in [4+1] cycloaddition with enones Organic Letters, 13, 15, 3837-3839 Organic Letters, 13, 15, 3837-3839 Organic Letters, 13, 15, 3837-3839 2011 Refereed English Disclose to all
T. Inami; T. Kurahashi; S. Matsubara T. Inami; T. Kurahashi; S. Matsubara T. Inami; T. Kurahashi; S. Matsubara Methylenecyclopropane as C1 synthetic units: [1+4] cycloaddition via a nickel catalyst Methylenecyclopropane as C1 synthetic units: [1+4] cycloaddition via a nickel catalyst Methylenecyclopropane as C1 synthetic units: [1+4] cycloaddition via a nickel catalyst Chemical Communications, 47, 34, 9711-9713 Chemical Communications, 47, 34, 9711-9713 Chemical Communications, 47, 34, 9711-9713 2011 Refereed English Disclose to all
M. Sai; S. Matsubara M. Sai; S. Matsubara M. Sai; S. Matsubara Silver-catalyzed intramolecular chloroamination of allenes: Easy access to functionalized 3-pyrroline and pyrrole derivatives Silver-catalyzed intramolecular chloroamination of allenes: Easy access to functionalized 3-pyrroline and pyrrole derivatives Silver-catalyzed intramolecular chloroamination of allenes: Easy access to functionalized 3-pyrroline and pyrrole derivatives Organic Letters, 13, 17, 4676-4679 Organic Letters, 13, 17, 4676-4679 Organic Letters, 13, 17, 4676-4679 2011 Refereed English Disclose to all
H. Horie; T. Kurahashi; S. Matsubara H. Horie; T. Kurahashi; S. Matsubara H. Horie; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of α,β,γ,δ- unsaturated ketones with alkynes Nickel-catalyzed cycloaddition of α,β,γ,δ- unsaturated ketones with alkynes Nickel-catalyzed cycloaddition of α,β,γ,δ- unsaturated ketones with alkynes Angewandte Chemie - International Edition, 50, 38, 8956-8959 Angewandte Chemie - International Edition, 50, 38, 8956-8959 Angewandte Chemie - International Edition, 50, 38, 8956-8959 2011 Refereed English Disclose to all
Y. Yoshida; T. Kurahashi; S. Matsubara Y. Yoshida; T. Kurahashi; S. Matsubara Y. Yoshida; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of aromatic (O-benzyl)ketoximes with alkynes to produce isoquinoline and isoquinoline N-oxide derivatives Nickel-catalyzed cycloaddition of aromatic (O-benzyl)ketoximes with alkynes to produce isoquinoline and isoquinoline N-oxide derivatives Nickel-catalyzed cycloaddition of aromatic (O-benzyl)ketoximes with alkynes to produce isoquinoline and isoquinoline N-oxide derivatives Chemistry Letters, 40, 10, 1140-1142 Chemistry Letters, 40, 10, 1140-1142 Chemistry Letters, 40, 10, 1140-1142 2011 Refereed English Disclose to all
Y. Yoshida; T. Kurahashi; S. Matsubara Y. Yoshida; T. Kurahashi; S. Matsubara Y. Yoshida; T. Kurahashi; S. Matsubara Nickel-catalyzed heteroannulation of o-haloanilines with alkynes Nickel-catalyzed heteroannulation of o-haloanilines with alkynes Nickel-catalyzed heteroannulation of o-haloanilines with alkynes Chemistry Letters, 40, 10, 1067-1068 Chemistry Letters, 40, 10, 1067-1068 Chemistry Letters, 40, 10, 1067-1068 2011 Refereed English Disclose to all
K. Nakai; T. Shiba; Y. Yoshino; T. Kurahashi; S. Matsubara K. Nakai; T. Shiba; Y. Yoshino; T. Kurahashi; S. Matsubara K. Nakai; T. Shiba; Y. Yoshino; T. Kurahashi; S. Matsubara Nickel-catalyzed decarboxylative polymerization of 6-alkynylisatoic anhydride Nickel-catalyzed decarboxylative polymerization of 6-alkynylisatoic anhydride Nickel-catalyzed decarboxylative polymerization of 6-alkynylisatoic anhydride Chemistry Letters, 40, 11, 1240-1241 Chemistry Letters, 40, 11, 1240-1241 Chemistry Letters, 40, 11, 1240-1241 2011 Refereed English Disclose to all
T. Ozawa; T. Kurahashi; S. Matsubara T. Ozawa; T. Kurahashi; S. Matsubara T. Ozawa; T. Kurahashi; S. Matsubara Dehydrogenative diels-alder reaction Dehydrogenative diels-alder reaction Dehydrogenative diels-alder reaction Organic Letters, 13, 19, 5390-5393 Organic Letters, 13, 19, 5390-5393 Organic Letters, 13, 19, 5390-5393 2011 Refereed English Disclose to all
M. Sada; S. Komagawa; M. Uchiyama; M. Kobata; T. Mizuno; K. Utimoto; K. Oshima; S. Matsubara M. Sada; S. Komagawa; M. Uchiyama; M. Kobata; T. Mizuno; K. Utimoto; K. Oshima; S. Matsubara M. Sada; S. Komagawa; M. Uchiyama; M. Kobata; T. Mizuno; K. Utimoto; K. Oshima; S. Matsubara Reaction pathway of methylenation of carbonyl compounds with bis(iodozincio)methane Reaction pathway of methylenation of carbonyl compounds with bis(iodozincio)methane Reaction pathway of methylenation of carbonyl compounds with bis(iodozincio)methane Journal of the American Chemical Society, 132, 49, 17452-17458 Journal of the American Chemical Society, 132, 49, 17452-17458 Journal of the American Chemical Society, 132, 49, 17452-17458 2010/12/15 Refereed English Disclose to all
T. Okamura; K. Asano; S. Matsubara T. Okamura; K. Asano; S. Matsubara T. Okamura; K. Asano; S. Matsubara Effects of a flexible alkyl chain on an imidazole ligand for copper-catalyzed mannich reactions of terminal alkynes Effects of a flexible alkyl chain on an imidazole ligand for copper-catalyzed mannich reactions of terminal alkynes Effects of a flexible alkyl chain on an imidazole ligand for copper-catalyzed mannich reactions of terminal alkynes Synlett, 20, 3053-3056 Synlett, 20, 3053-3056 Synlett, 20, 3053-3056 2010/12 Refereed English Disclose to all
Y. Takada; K. Nomura; S. Matsubara Y. Takada; K. Nomura; S. Matsubara Y. Takada; K. Nomura; S. Matsubara Preparation of a cycloheptane ring from a 1,2-diketone with high stereoselectivity Preparation of a cycloheptane ring from a 1,2-diketone with high stereoselectivity Preparation of a cycloheptane ring from a 1,2-diketone with high stereoselectivity Organic Letters, 12, 22, 5204-5205 Organic Letters, 12, 22, 5204-5205 Organic Letters, 12, 22, 5204-5205 2010/11/19 Refereed English Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara Effects of a flexible alkyl chain on a ligand for CuAAC reaction Effects of a flexible alkyl chain on a ligand for CuAAC reaction Effects of a flexible alkyl chain on a ligand for CuAAC reaction Organic Letters, 12, 21, 4988-4991 Organic Letters, 12, 21, 4988-4991 Organic Letters, 12, 21, 4988-4991 2010/11/05 Refereed English Disclose to all
K. Fujiwara; T. Kurahashi; S. Matsubara K. Fujiwara; T. Kurahashi; S. Matsubara K. Fujiwara; T. Kurahashi; S. Matsubara Decarbonylative cycloaddition of phthalimides with 1,3-dienes Decarbonylative cycloaddition of phthalimides with 1,3-dienes Decarbonylative cycloaddition of phthalimides with 1,3-dienes Organic Letters, 12, 20, 4548-4551 Organic Letters, 12, 20, 4548-4551 Organic Letters, 12, 20, 4548-4551 2010/10/15 Refereed English Disclose to all
Y. Yoshino; T. Kurahashi; S. Matsubara Y. Yoshino; T. Kurahashi; S. Matsubara Y. Yoshino; T. Kurahashi; S. Matsubara Nickel-catalyzed [4 + 2] cycloaddition of alkynes to carbonylsalicylamides via elimination of isocyanates Nickel-catalyzed [4 + 2] cycloaddition of alkynes to carbonylsalicylamides via elimination of isocyanates Nickel-catalyzed [4 + 2] cycloaddition of alkynes to carbonylsalicylamides via elimination of isocyanates Chemistry Letters, 39, 8, 896-897 Chemistry Letters, 39, 8, 896-897 Chemistry Letters, 39, 8, 896-897 2010/08/05 Refereed English Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara Design of reaction media for nucleophilic substitution reactions by using a catalytic amount of an amphiphilic imidazolium salt in water Design of reaction media for nucleophilic substitution reactions by using a catalytic amount of an amphiphilic imidazolium salt in water Design of reaction media for nucleophilic substitution reactions by using a catalytic amount of an amphiphilic imidazolium salt in water Heterocycles, 80, 2, 989-1002 Heterocycles, 80, 2, 989-1002 Heterocycles, 80, 2, 989-1002 2010/03/01 Refereed English Disclose to all
S. Ueno; M. Sada; S. Matsubara S. Ueno; M. Sada; S. Matsubara S. Ueno; M. Sada; S. Matsubara Preparation of ester-group substituted allylic zinc by palladium-catalyzed umpolung of γ-acyloxy-α,β-unsaturated ester by bis(iodozincio)methane Preparation of ester-group substituted allylic zinc by palladium-catalyzed umpolung of γ-acyloxy-α,β-unsaturated ester by bis(iodozincio)methane Preparation of ester-group substituted allylic zinc by palladium-catalyzed umpolung of γ-acyloxy-α,β-unsaturated ester by bis(iodozincio)methane Chemistry Letters, 39, 2, 96-97 Chemistry Letters, 39, 2, 96-97 Chemistry Letters, 39, 2, 96-97 2010/02/05 Refereed English Disclose to all
M. Sada; S. Matsubara M. Sada; S. Matsubara M. Sada; S. Matsubara A tandem reaction initiated by 1,4-addition of bis(iodozincio)methane for 1,3-diketone formation A tandem reaction initiated by 1,4-addition of bis(iodozincio)methane for 1,3-diketone formation A tandem reaction initiated by 1,4-addition of bis(iodozincio)methane for 1,3-diketone formation Journal of the American Chemical Society, 132, 2, 432-+ Journal of the American Chemical Society, 132, 2, 432-+ Journal of the American Chemical Society, 132, 2, 432-+ 2010/01/20 Refereed English Disclose to all
K. Nomura; S. Matsubara K. Nomura; S. Matsubara K. Nomura; S. Matsubara Stereospecific construction of chiral tertiary and quaternary carbon by nucleophilic cyclopropanation with bis(iodozincio)methane Stereospecific construction of chiral tertiary and quaternary carbon by nucleophilic cyclopropanation with bis(iodozincio)methane Stereospecific construction of chiral tertiary and quaternary carbon by nucleophilic cyclopropanation with bis(iodozincio)methane Chemistry - An Asian Journal, 5, 1, 147-152 Chemistry - An Asian Journal, 5, 1, 147-152 Chemistry - An Asian Journal, 5, 1, 147-152 2010 Refereed English Disclose to all
K. Nomura; S. Matsubara K. Nomura; S. Matsubara K. Nomura; S. Matsubara A new zincate-mediated rearrangement reaction of 2-(1-hydroxyalkyl)-1- alkylcyclopropanol A new zincate-mediated rearrangement reaction of 2-(1-hydroxyalkyl)-1- alkylcyclopropanol A new zincate-mediated rearrangement reaction of 2-(1-hydroxyalkyl)-1- alkylcyclopropanol Chemistry - A European Journal, 16, 2, 703-708 Chemistry - A European Journal, 16, 2, 703-708 Chemistry - A European Journal, 16, 2, 703-708 2010 Refereed English Disclose to all
H. Horie; T. Kurahashi; S. Matsubara H. Horie; T. Kurahashi; S. Matsubara H. Horie; T. Kurahashi; S. Matsubara Selective synthesis of trienes and dienes via nickel-catalyzed intermolecular cotrimerization of acrylates and alkynes Selective synthesis of trienes and dienes via nickel-catalyzed intermolecular cotrimerization of acrylates and alkynes Selective synthesis of trienes and dienes via nickel-catalyzed intermolecular cotrimerization of acrylates and alkynes Chemical Communications, 46, 38, 7229-7231 Chemical Communications, 46, 38, 7229-7231 Chemical Communications, 46, 38, 7229-7231 2010 Refereed English Disclose to all
M. Sada; T. Furayama; S. Komagawa; M. Uchiyama; S. Matsubara M. Sada; T. Furayama; S. Komagawa; M. Uchiyama; S. Matsubara M. Sada; T. Furayama; S. Komagawa; M. Uchiyama; S. Matsubara 1,4-Addition of Bis(iodozincio)methane to α,β-Unsaturated ketones: Chemical and theoretical/computational studies 1,4-Addition of Bis(iodozincio)methane to α,β-Unsaturated ketones: Chemical and theoretical/computational studies 1,4-Addition of Bis(iodozincio)methane to α,β-Unsaturated ketones: Chemical and theoretical/computational studies Chemistry - A European Journal, 16, 34, 10474-10481 Chemistry - A European Journal, 16, 34, 10474-10481 Chemistry - A European Journal, 16, 34, 10474-10481 2010 Refereed English Disclose to all
T. Ozawa; H. Horie; T. Kurahashi; S. Matsubara T. Ozawa; H. Horie; T. Kurahashi; S. Matsubara T. Ozawa; H. Horie; T. Kurahashi; S. Matsubara Nickel-catalyzed [2+2+1] cycloaddition of alkynes, acrylates and isocyanates Nickel-catalyzed [2+2+1] cycloaddition of alkynes, acrylates and isocyanates Nickel-catalyzed [2+2+1] cycloaddition of alkynes, acrylates and isocyanates Chemical Communications, 46, 42, 8055-8057 Chemical Communications, 46, 42, 8055-8057 Chemical Communications, 46, 42, 8055-8057 2010 Refereed English Disclose to all
T. Kurahashi; S. Matsubara T. Kurahashi; S. Matsubara Syntheses of heterocycles by nickel-catalyzed substitution reaction -development of [6-2+2] reaction- Syntheses of heterocycles by nickel-catalyzed substitution reaction -development of [6-2+2] reaction- Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 68, 1, 33-40 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 68, 1, 33-40 , 68, 1, 33-40 2010 Refereed Japanese Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara Morita-baylis-hillman reaction on water without organic solvent, assisted by a \\'catalytic\\' amount of amphiphilic imidazole derivatives Morita-baylis-hillman reaction on water without organic solvent, assisted by a \\'catalytic\\' amount of amphiphilic imidazole derivatives Morita-baylis-hillman reaction on water without organic solvent, assisted by a \\'catalytic\\' amount of amphiphilic imidazole derivatives Synthesis, 19, 3219-3226 Synthesis, 19, 3219-3226 Synthesis, 19, 3219-3226 2009/10/01 Refereed English Disclose to all
A. Ooguri; K. Nakai; T. Kurahashi; S. Matsubara A. Ooguri; K. Nakai; T. Kurahashi; S. Matsubara A. Ooguri; K. Nakai; T. Kurahashi; S. Matsubara Nickel-catalyzed cycloaddition of salicylic acid ketals to alkynes via elimination of ketones Nickel-catalyzed cycloaddition of salicylic acid ketals to alkynes via elimination of ketones Nickel-catalyzed cycloaddition of salicylic acid ketals to alkynes via elimination of ketones Journal of the American Chemical Society, 131, 37, 13194-+ Journal of the American Chemical Society, 131, 37, 13194-+ Journal of the American Chemical Society, 131, 37, 13194-+ 2009/09/23 Refereed English Disclose to all
Y. Yoshino; T. Kurahashi; S. Matsubara Y. Yoshino; T. Kurahashi; S. Matsubara Y. Yoshino; T. Kurahashi; S. Matsubara Nickel-catalyzed decarboxylative carboamination of alkynes with isatoic anhydrides Nickel-catalyzed decarboxylative carboamination of alkynes with isatoic anhydrides Nickel-catalyzed decarboxylative carboamination of alkynes with isatoic anhydrides Journal of the American Chemical Society, 131, 22, 7494-+ Journal of the American Chemical Society, 131, 22, 7494-+ Journal of the American Chemical Society, 131, 22, 7494-+ 2009/06/10 Refereed English Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara Amphiphilic organocatalyst for schotten-baumann-type tosylation of alcohols under organic solvent free condition Amphiphilic organocatalyst for schotten-baumann-type tosylation of alcohols under organic solvent free condition Amphiphilic organocatalyst for schotten-baumann-type tosylation of alcohols under organic solvent free condition Organic Letters, 11, 8, 1757-1759 Organic Letters, 11, 8, 1757-1759 Organic Letters, 11, 8, 1757-1759 2009/04/16 Refereed English Disclose to all
M. Sada; S. Ueno; K. Asano; K. Nomura; S. Matsubara M. Sada; S. Ueno; K. Asano; K. Nomura; S. Matsubara M. Sada; S. Ueno; K. Asano; K. Nomura; S. Matsubara Stereoselective preparation of 3-alkanoylprop-2-en-1-ol derivatives Stereoselective preparation of 3-alkanoylprop-2-en-1-ol derivatives Stereoselective preparation of 3-alkanoylprop-2-en-1-ol derivatives Synlett, 5, 724-726 Synlett, 5, 724-726 Synlett, 5, 724-726 2009/03/17 Refereed English Disclose to all
H. Horie; Y. Kajita; S. Matsubara H. Horie; Y. Kajita; S. Matsubara H. Horie; Y. Kajita; S. Matsubara Sequential introduction of carbon nucleophiles onto silicon atoms using methyl as a leaving group Sequential introduction of carbon nucleophiles onto silicon atoms using methyl as a leaving group Sequential introduction of carbon nucleophiles onto silicon atoms using methyl as a leaving group Chemistry Letters, 38, 2, 116-117 Chemistry Letters, 38, 2, 116-117 Chemistry Letters, 38, 2, 116-117 2009/02/05 Refereed English Disclose to all
I. Koyama; T. Kurahashi; S. Matsubara I. Koyama; T. Kurahashi; S. Matsubara I. Koyama; T. Kurahashi; S. Matsubara Nickel-catalyzed [4 + 2] cycloaddition of enones with alkynes Nickel-catalyzed [4 + 2] cycloaddition of enones with alkynes Nickel-catalyzed [4 + 2] cycloaddition of enones with alkynes Journal of the American Chemical Society, 131, 4, 1350-+ Journal of the American Chemical Society, 131, 4, 1350-+ Journal of the American Chemical Society, 131, 4, 1350-+ 2009/02/04 Refereed English Disclose to all
K. Asano; S. Matsubara K. Asano; S. Matsubara K. Asano; S. Matsubara N-alkylimidazole as amphiphilic organocatalyst: \\'Catalytic\\' Morita-Baylis-Hillman reaction on water without organic solvent N-alkylimidazole as amphiphilic organocatalyst: \\'Catalytic\\' Morita-Baylis-Hillman reaction on water without organic solvent N-alkylimidazole as amphiphilic organocatalyst: \\'Catalytic\\' Morita-Baylis-Hillman reaction on water without organic solvent Synlett, 1, 35-38 Synlett, 1, 35-38 Synlett, 1, 35-38 2009/01/02 Refereed English Disclose to all
K. Nomura; S. Matsubara K. Nomura; S. Matsubara K. Nomura; S. Matsubara Zincate-mediated rearrangement reaction of 2-(1-hydroxyalkyl)-1- alkylcyclopropanol Zincate-mediated rearrangement reaction of 2-(1-hydroxyalkyl)-1- alkylcyclopropanol Zincate-mediated rearrangement reaction of 2-(1-hydroxyalkyl)-1- alkylcyclopropanol Chemical Communications, 16, 2212-2213 Chemical Communications, 16, 2212-2213 Chemical Communications, 16, 2212-2213 2009 Refereed English Disclose to all
K. Nomura; T. Hirayama; S. Matsubara K. Nomura; T. Hirayama; S. Matsubara K. Nomura; T. Hirayama; S. Matsubara Nucleophilic cyclopropanation reaction with bis(iodozincio)methane by 1,4-addition to α,β-unsaturated carbonyl compounds Nucleophilic cyclopropanation reaction with bis(iodozincio)methane by 1,4-addition to α,β-unsaturated carbonyl compounds Nucleophilic cyclopropanation reaction with bis(iodozincio)methane by 1,4-addition to α,β-unsaturated carbonyl compounds Chemistry - An Asian Journal, 4, 8, 1298-1303 Chemistry - An Asian Journal, 4, 8, 1298-1303 Chemistry - An Asian Journal, 4, 8, 1298-1303 2009 Refereed English Disclose to all
Y. Kajita; T. Kurahashi; S. Matsubara Y. Kajita; T. Kurahashi; S. Matsubara Y. Kajita; T. Kurahashi; S. Matsubara Nickel-catalyzed decarbonylative addition of anhydrides to alkynes Nickel-catalyzed decarbonylative addition of anhydrides to alkynes Nickel-catalyzed decarbonylative addition of anhydrides to alkynes Journal of the American Chemical Society, 130, 51, 17226-+ Journal of the American Chemical Society, 130, 51, 17226-+ Journal of the American Chemical Society, 130, 51, 17226-+ 2008/12/24 Refereed English Disclose to all
K. Nomura; K. Asano; T. Kurahashi; S. Matsubara K. Nomura; K. Asano; T. Kurahashi; S. Matsubara K. Nomura; K. Asano; T. Kurahashi; S. Matsubara Diastereoselective nucleophilic cyclopropanation of 1,2-diketones and α-ketoimines with bis(iodozincio)methane Diastereoselective nucleophilic cyclopropanation of 1,2-diketones and α-ketoimines with bis(iodozincio)methane Diastereoselective nucleophilic cyclopropanation of 1,2-diketones and α-ketoimines with bis(iodozincio)methane Heterocycles, 76, 2, 1381-1399 Heterocycles, 76, 2, 1381-1399 Heterocycles, 76, 2, 1381-1399 2008/11/01 Refereed English Disclose to all
Y. Baba; A. Toshimitsu; S. Matsubara Y. Baba; A. Toshimitsu; S. Matsubara Y. Baba; A. Toshimitsu; S. Matsubara Nickel-catalyzed cross-coupling reaction of allyl- and benzylzinc with alkenyl sulfides Nickel-catalyzed cross-coupling reaction of allyl- and benzylzinc with alkenyl sulfides Nickel-catalyzed cross-coupling reaction of allyl- and benzylzinc with alkenyl sulfides Synlett, 13, 2061-2063 Synlett, 13, 2061-2063 Synlett, 13, 2061-2063 2008/08 Refereed English Disclose to all
S. Yagi; H. Nakanishi; E. Matsubara; S. Matsubara; T. Ichitsubo; K. Hosoya; Y. Matsuba S. Yagi; H. Nakanishi; E. Matsubara; S. Matsubara; T. Ichitsubo; K. Hosoya; Y. Matsuba S. Yagi; H. Nakanishi; E. Matsubara; S. Matsubara; T. Ichitsubo; K. Hosoya; Y. Matsuba Formation of Cu nanoparticles by electroless deposition using aqueous CuO suspension Formation of Cu nanoparticles by electroless deposition using aqueous CuO suspension Formation of Cu nanoparticles by electroless deposition using aqueous CuO suspension Journal of the Electrochemical Society, 155, 6, D474-D479 Journal of the Electrochemical Society, 155, 6, D474-D479 Journal of the Electrochemical Society, 155, 6, D474-D479 2008 Refereed English Disclose to all
Y. Kajita; S. Matsubara; T. Kurahashi Y. Kajita; S. Matsubara; T. Kurahashi Y. Kajita; S. Matsubara; T. Kurahashi Nickel-catalyzed decarbonylative addition of phthalimides to alkynes Nickel-catalyzed decarbonylative addition of phthalimides to alkynes Nickel-catalyzed decarbonylative addition of phthalimides to alkynes Journal of the American Chemical Society, 130, 19, 6058-6059 Journal of the American Chemical Society, 130, 19, 6058-6059 Journal of the American Chemical Society, 130, 19, 6058-6059 2008 Refereed English Disclose to all
K. Nomura; S. Matsubara K. Nomura; S. Matsubara K. Nomura; S. Matsubara Stereoselective synthesis of β,γ-unsaturated ketones by acid-mediated Julia-type transformation from 2-(1-hydroxyalkyl)-1- alkylcyclopropanols Stereoselective synthesis of β,γ-unsaturated ketones by acid-mediated Julia-type transformation from 2-(1-hydroxyalkyl)-1- alkylcyclopropanols Stereoselective synthesis of β,γ-unsaturated ketones by acid-mediated Julia-type transformation from 2-(1-hydroxyalkyl)-1- alkylcyclopropanols Synlett, 9, 1412-1414 Synlett, 9, 1412-1414 Synlett, 9, 1412-1414 2008 Refereed English Disclose to all
M. Sada; S. Matsubara M. Sada; S. Matsubara M. Sada; S. Matsubara Iron(II) chloride-mediated addition of dialkylmagnesium to carbonyl compounds Iron(II) chloride-mediated addition of dialkylmagnesium to carbonyl compounds Iron(II) chloride-mediated addition of dialkylmagnesium to carbonyl compounds Chemistry Letters, 37, 7, 800-801 Chemistry Letters, 37, 7, 800-801 Chemistry Letters, 37, 7, 800-801 2008 Refereed English Disclose to all
S. Matsubara S. Matsubara S. Matsubara Polyfunctional 1,1-Organodimetallic for Organic Synthesis Polyfunctional 1,1-Organodimetallic for Organic Synthesis Polyfunctional 1,1-Organodimetallic for Organic Synthesis Handbook of Functionalized Organometallics: Applications in Synthesis, 2, 347-377 Handbook of Functionalized Organometallics: Applications in Synthesis, 2, 347-377 Handbook of Functionalized Organometallics: Applications in Synthesis, 2, 347-377 2008 Refereed English Disclose to all
S.-I. Murahashi; Y. Yamamoto; G.B. Bajracharya; C. Nicolau; M. Oiarbide; Y. Hamashima; M. Sodeoka; A. Córdova; B.B. Snider; T. Yoshimitsu; F. Minisci; O. Porta; B.M. Stoltz; D.C. Ebner; A. Ganesan; S. Kaskel; J.A. Varela; G. Dyker; A. Christiansen; A. Börner; S. Matsubara; J.-C. Frison; J. Legros; C. Bolm; M. He; A. Lei; X. Zhang; B. Sezen; D. Sames S.-I. Murahashi; Y. Yamamoto; G.B. Bajracharya; C. Nicolau; M. Oiarbide; Y. Hamashima; M. Sodeoka; A. Córdova; B.B. Snider; T. Yoshimitsu; F. Minisci; O. Porta; B.M. Stoltz; D.C. Ebner; A. Ganesan; S. Kaskel; J.A. Varela; G. Dyker; A. Christiansen; A. Börner; S. Matsubara; J.-C. Frison; J. Legros; C. Bolm; M. He; A. Lei; X. Zhang; B. Sezen; D. Sames S.-I. Murahashi; Y. Yamamoto; G.B. Bajracharya; C. Nicolau; M. Oiarbide; Y. Hamashima; M. Sodeoka; A. Córdova; B.B. Snider; T. Yoshimitsu; F. Minisci; O. Porta; B.M. Stoltz; D.C. Ebner; A. Ganesan; S. Kaskel; J.A. Varela; G. Dyker; A. Christiansen; A. Börner; S. Matsubara; J.-C. Frison; J. Legros; C. Bolm; M. He; A. Lei; X. Zhang; B. Sezen; D. Sames C-H Transformation at Functionalized Alkanes C-H Transformation at Functionalized Alkanes C-H Transformation at Functionalized Alkanes Handbook of C-H Transformations: Applications in Organic Synthesis, 2, 317-496 Handbook of C-H Transformations: Applications in Organic Synthesis, 2, 317-496 Handbook of C-H Transformations: Applications in Organic Synthesis, 2, 317-496 2008 Refereed English Disclose to all
S. Yagi; T. Nakagawa; E. Matsubara; S. Matsubara; S. Ogawa; H. Tani S. Yagi; T. Nakagawa; E. Matsubara; S. Matsubara; S. Ogawa; H. Tani S. Yagi; T. Nakagawa; E. Matsubara; S. Matsubara; S. Ogawa; H. Tani Formation of tin nanoparticles embedded in Poly(L-Lactic acid) fiber by electrospinning Formation of tin nanoparticles embedded in Poly(L-Lactic acid) fiber by electrospinning Formation of tin nanoparticles embedded in Poly(L-Lactic acid) fiber by electrospinning Electrochemical and Solid-State Letters, 11, 9, E25-E27 Electrochemical and Solid-State Letters, 11, 9, E25-E27 Electrochemical and Solid-State Letters, 11, 9, E25-E27 2008 Refereed English Disclose to all
Y. Baba; A. Toshimitsu; S. Matsubara Y. Baba; A. Toshimitsu; S. Matsubara Y. Baba; A. Toshimitsu; S. Matsubara Preparation and reaction of phenylsulfonyl-substituted dizinciomethane Preparation and reaction of phenylsulfonyl-substituted dizinciomethane Preparation and reaction of phenylsulfonyl-substituted dizinciomethane Chemistry Letters, 36, 7, 864-865 Chemistry Letters, 36, 7, 864-865 Chemistry Letters, 36, 7, 864-865 2007/07/05 Refereed English Disclose to all
S. Matsubara; K. Asano; Y. Kajita; M. Yamamoto S. Matsubara; K. Asano; Y. Kajita; M. Yamamoto S. Matsubara; K. Asano; Y. Kajita; M. Yamamoto C-H bond activation by water on a palladium or platinum metal surface C-H bond activation by water on a palladium or platinum metal surface C-H bond activation by water on a palladium or platinum metal surface Synthesis, 13, 2055-2059 Synthesis, 13, 2055-2059 Synthesis, 13, 2055-2059 2007/07/03 Refereed English Disclose to all
M. Yamamoto; S. Matsubara M. Yamamoto; S. Matsubara M. Yamamoto; S. Matsubara Carbazole synthesis by platinum-catalyzed C-H functionalizing reaction using water as reoxidizing reagent Carbazole synthesis by platinum-catalyzed C-H functionalizing reaction using water as reoxidizing reagent Carbazole synthesis by platinum-catalyzed C-H functionalizing reaction using water as reoxidizing reagent Chemistry Letters, 36, 1, 172-173 Chemistry Letters, 36, 1, 172-173 Chemistry Letters, 36, 1, 172-173 2007 Refereed English Disclose to all
K. Nomura; S. Matsubara K. Nomura; S. Matsubara K. Nomura; S. Matsubara Preparation of zinc-homoenolate from α-sulfonyloxy ketone and bis(iodozincio)methane Preparation of zinc-homoenolate from α-sulfonyloxy ketone and bis(iodozincio)methane Preparation of zinc-homoenolate from α-sulfonyloxy ketone and bis(iodozincio)methane Chemistry Letters, 36, 1, 164-165 Chemistry Letters, 36, 1, 164-165 Chemistry Letters, 36, 1, 164-165 2007 Refereed English Disclose to all
K. Ishibashi; S. Matsubara K. Ishibashi; S. Matsubara K. Ishibashi; S. Matsubara Preparation of cyclohexene-d<sub>10</sub> by H/D-exchange reaction Preparation of cyclohexene-d<sub>10</sub> by H/D-exchange reaction Preparation of cyclohexene-d<sub>10</sub> by H/D-exchange reaction Chemistry Letters, 36, 6, 724-725 Chemistry Letters, 36, 6, 724-725 Chemistry Letters, 36, 6, 724-725 2007 Refereed English Disclose to all
A. Ooguri; Z. Ikeda; S. Matsubara A. Ooguri; Z. Ikeda; S. Matsubara A. Ooguri; Z. Ikeda; S. Matsubara Chemo-, regio- and stereoselective preparation of silyl enol ethers from thiol esters and bis(iodozincio)alkane Chemo-, regio- and stereoselective preparation of silyl enol ethers from thiol esters and bis(iodozincio)alkane Chemo-, regio- and stereoselective preparation of silyl enol ethers from thiol esters and bis(iodozincio)alkane Chemical Communications, 45, 4761-4763 Chemical Communications, 45, 4761-4763 Chemical Communications, 45, 4761-4763 2007 Refereed English Disclose to all
S. Matsubara S. Matsubara Transition of methylenation reaction- The outcome of "ingredients of couldron" Transition of methylenation reaction- The outcome of "ingredients of couldron" Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 65, 3, 194-203 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 65, 3, 194-203 , 65, 3, 194-203 2007 Refereed Japanese Disclose to all
K. Matsumoto; J. Ohtsuki; R. Hagiwara; S. Matsubara K. Matsumoto; J. Ohtsuki; R. Hagiwara; S. Matsubara K. Matsumoto; J. Ohtsuki; R. Hagiwara; S. Matsubara Cesium fluorohydrogenate, Cs(FH)<sub>2.3</sub>F Cesium fluorohydrogenate, Cs(FH)<sub>2.3</sub>F Cesium fluorohydrogenate, Cs(FH)<sub>2.3</sub>F Journal of Fluorine Chemistry, 127, 10, 1339-1343 Journal of Fluorine Chemistry, 127, 10, 1339-1343 Journal of Fluorine Chemistry, 127, 10, 1339-1343 2006/10 Refereed English Disclose to all
H. Yoshino; N. Toda; M. Kobata; K. Ukai; K. Oshima; K. Utimoto; S. Matsubara H. Yoshino; N. Toda; M. Kobata; K. Ukai; K. Oshima; K. Utimoto; S. Matsubara H. Yoshino; N. Toda; M. Kobata; K. Ukai; K. Oshima; K. Utimoto; S. Matsubara Transition-metal-catalyzed sequential cross-coupling of bis(iodozincio)methane and -ethane with two different organic halides Transition-metal-catalyzed sequential cross-coupling of bis(iodozincio)methane and -ethane with two different organic halides Transition-metal-catalyzed sequential cross-coupling of bis(iodozincio)methane and -ethane with two different organic halides Chemistry - A European Journal, 12, 3, 721-726 Chemistry - A European Journal, 12, 3, 721-726 Chemistry - A European Journal, 12, 3, 721-726 2006/01/11 Refereed English Disclose to all
M. Yamamoto; K. Oshima; S. Matsubara M. Yamamoto; K. Oshima; S. Matsubara M. Yamamoto; K. Oshima; S. Matsubara Platinum catalyzed H-D exchange reaction of various aromatic compounds under hydrothermal condition Platinum catalyzed H-D exchange reaction of various aromatic compounds under hydrothermal condition Platinum catalyzed H-D exchange reaction of various aromatic compounds under hydrothermal condition Heterocycles, 67, 1, 353-359 Heterocycles, 67, 1, 353-359 Heterocycles, 67, 1, 353-359 2006/01/01 Refereed English Disclose to all
H. Yoshino; K. Matsumoto; R. Hagiwara; Y. Ito; K. Oshima; S. Matsubara H. Yoshino; K. Matsumoto; R. Hagiwara; Y. Ito; K. Oshima; S. Matsubara H. Yoshino; K. Matsumoto; R. Hagiwara; Y. Ito; K. Oshima; S. Matsubara Fluorination with ionic liquid EMIMF(HF)<sub>2.3</sub> as mild HF source Fluorination with ionic liquid EMIMF(HF)<sub>2.3</sub> as mild HF source Fluorination with ionic liquid EMIMF(HF)<sub>2.3</sub> as mild HF source Journal of Fluorine Chemistry, 127, 1, 29-35 Journal of Fluorine Chemistry, 127, 1, 29-35 Journal of Fluorine Chemistry, 127, 1, 29-35 2006/01 Refereed English Disclose to all
Z. Ikeda; T. Hirayama; S. Matsubara Z. Ikeda; T. Hirayama; S. Matsubara Z. Ikeda; T. Hirayama; S. Matsubara Chemo- and regioselective preparation and reaction of a kinetic zinc enolate formed from a thiol ester and bis(iodozincio)methane Chemo- and regioselective preparation and reaction of a kinetic zinc enolate formed from a thiol ester and bis(iodozincio)methane Chemo- and regioselective preparation and reaction of a kinetic zinc enolate formed from a thiol ester and bis(iodozincio)methane Angewandte Chemie - International Edition, 45, 48, 8200-8203 Angewandte Chemie - International Edition, 45, 48, 8200-8203 Angewandte Chemie - International Edition, 45, 48, 8200-8203 2006 Refereed English Disclose to all
S. Horike; R. Matsuda; D. Tanaka; S. Matsubara; M. Mizuno; K. Endo; S. Kitagawa S. Horike; R. Matsuda; D. Tanaka; S. Matsubara; M. Mizuno; K. Endo; S. Kitagawa S. Horike; R. Matsuda; D. Tanaka; S. Matsubara; M. Mizuno; K. Endo; S. Kitagawa Dynamic motion of building blocks in porous coordination polymers Dynamic motion of building blocks in porous coordination polymers Dynamic motion of building blocks in porous coordination polymers Angewandte Chemie - International Edition, 45, 43, 7226-7230 Angewandte Chemie - International Edition, 45, 43, 7226-7230 Angewandte Chemie - International Edition, 45, 43, 7226-7230 2006 Refereed English Disclose to all
S. Matsubara; H. Yoshino; Y. Yamamoto; K. Oshima; H. Matsuoka; K. Matsumoto; K. Ishikawa; E. Matsubara S. Matsubara; H. Yoshino; Y. Yamamoto; K. Oshima; H. Matsuoka; K. Matsumoto; K. Ishikawa; E. Matsubara S. Matsubara; H. Yoshino; Y. Yamamoto; K. Oshima; H. Matsuoka; K. Matsumoto; K. Ishikawa; E. Matsubara Structure and reactivity of bis(iodozincio)methane solution Structure and reactivity of bis(iodozincio)methane solution Structure and reactivity of bis(iodozincio)methane solution Journal of Organometallic Chemistry, 690, 24-25, 5546-5551 Journal of Organometallic Chemistry, 690, 24-25, 5546-5551 Journal of Organometallic Chemistry, 690, 24-25, 5546-5551 2005/12/01 Refereed English Disclose to all
Z. Ikeda; K. Oshima; S. Matsubara Z. Ikeda; K. Oshima; S. Matsubara Z. Ikeda; K. Oshima; S. Matsubara Preparation and reaction of 2-aryl-3-silyl-1,3-butadiene Preparation and reaction of 2-aryl-3-silyl-1,3-butadiene Preparation and reaction of 2-aryl-3-silyl-1,3-butadiene Organic Letters, 7, 22, 4859-4861 Organic Letters, 7, 22, 4859-4861 Organic Letters, 7, 22, 4859-4861 2005/10/27 Refereed English Disclose to all
S. Matsubara; K. Oshima; H. Matsuoka; K. Matsumoto; K. Ishikawa; E. Matsubara S. Matsubara; K. Oshima; H. Matsuoka; K. Matsumoto; K. Ishikawa; E. Matsubara S. Matsubara; K. Oshima; H. Matsuoka; K. Matsumoto; K. Ishikawa; E. Matsubara Structure of bis(iodozincio)methane in THF solution Structure of bis(iodozincio)methane in THF solution Structure of bis(iodozincio)methane in THF solution Chemistry Letters, 34, 7, 952-953 Chemistry Letters, 34, 7, 952-953 Chemistry Letters, 34, 7, 952-953 2005/07/05 Refereed English Disclose to all
K. Ishibashi; M. Takahashi; Y. Yokota; K. Oshima; S. Matsubara K. Ishibashi; M. Takahashi; Y. Yokota; K. Oshima; S. Matsubara K. Ishibashi; M. Takahashi; Y. Yokota; K. Oshima; S. Matsubara Ruthenium-catalyzed isomerization of alkenol into alkanone in water under irradiation of microwaves Ruthenium-catalyzed isomerization of alkenol into alkanone in water under irradiation of microwaves Ruthenium-catalyzed isomerization of alkenol into alkanone in water under irradiation of microwaves Chemistry Letters, 34, 5, 664-665 Chemistry Letters, 34, 5, 664-665 Chemistry Letters, 34, 5, 664-665 2005/05/05 Refereed English Disclose to all
M. Takahashi; K. Oshima; S. Matsubara M. Takahashi; K. Oshima; S. Matsubara M. Takahashi; K. Oshima; S. Matsubara Ruthenium catalyzed deuterium labelling of α-carbon in primary alcohol and primary/secondary amine in D<sub>2</sub>O Ruthenium catalyzed deuterium labelling of α-carbon in primary alcohol and primary/secondary amine in D<sub>2</sub>O Ruthenium catalyzed deuterium labelling of α-carbon in primary alcohol and primary/secondary amine in D<sub>2</sub>O Chemistry Letters, 34, 2, 192-193 Chemistry Letters, 34, 2, 192-193 Chemistry Letters, 34, 2, 192-193 2005/02/05 Refereed English Disclose to all
S. Matsubara; K. Oshima S. Matsubara; K. Oshima S. Matsubara; K. Oshima Story concerning about autoclave -H-D exchange reaction of organic compounds in deuterium oxide under supercritical condition, hydrothermal condition, or microwave irradiation Story concerning about autoclave -H-D exchange reaction of organic compounds in deuterium oxide under supercritical condition, hydrothermal condition, or microwave irradiation Story concerning about autoclave -H-D exchange reaction of organic compounds in deuterium oxide under supercritical condition, hydrothermal condition, or microwave irradiation Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 63, 2, 154-161 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 63, 2, 154-161 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 63, 2, 154-161 2005/02 Refereed Other Disclose to all
H. Yoshino; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito H. Yoshino; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito H. Yoshino; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito A mild method for halofluorination of alkenes with ionic liquid EMIMF(HF) <sub>2.3</sub> A mild method for halofluorination of alkenes with ionic liquid EMIMF(HF) <sub>2.3</sub> A mild method for halofluorination of alkenes with ionic liquid EMIMF(HF) <sub>2.3</sub> Journal of Fluorine Chemistry, 126, 1, 121-123 Journal of Fluorine Chemistry, 126, 1, 121-123 Journal of Fluorine Chemistry, 126, 1, 121-123 2005/01 Refereed English Disclose to all
T. Hirayama; K. Oshima; S. Matsubara T. Hirayama; K. Oshima; S. Matsubara T. Hirayama; K. Oshima; S. Matsubara Preparation of enolate-homoenolate species as (Z)-γ-siloxyallylmetal equivalents: Sequential 1,4-addition of Bis(iodozincio)methane to 1,4-dicarbonylbutenes and cyclopropanation Preparation of enolate-homoenolate species as (Z)-γ-siloxyallylmetal equivalents: Sequential 1,4-addition of Bis(iodozincio)methane to 1,4-dicarbonylbutenes and cyclopropanation Preparation of enolate-homoenolate species as (Z)-γ-siloxyallylmetal equivalents: Sequential 1,4-addition of Bis(iodozincio)methane to 1,4-dicarbonylbutenes and cyclopropanation Angewandte Chemie - International Edition, 44, 21, 3293-3296 Angewandte Chemie - International Edition, 44, 21, 3293-3296 Angewandte Chemie - International Edition, 44, 21, 3293-3296 2005 Refereed English Disclose to all
K. Nomura; K. Oshima; S. Matsubara K. Nomura; K. Oshima; S. Matsubara K. Nomura; K. Oshima; S. Matsubara Stereospecific and stereoselective preparation of 2-(1-hydroxyalkyl)-1- alkylcyclopropanols from α,β-epoxy ketones and bis(iodozincio)methane Stereospecific and stereoselective preparation of 2-(1-hydroxyalkyl)-1- alkylcyclopropanols from α,β-epoxy ketones and bis(iodozincio)methane Stereospecific and stereoselective preparation of 2-(1-hydroxyalkyl)-1- alkylcyclopropanols from α,β-epoxy ketones and bis(iodozincio)methane Angewandte Chemie - International Edition, 44, 36, 5860-5863 Angewandte Chemie - International Edition, 44, 36, 5860-5863 Angewandte Chemie - International Edition, 44, 36, 5860-5863 2005 Refereed English Disclose to all
松原誠二郎 (大学院工学研究科助教授) 松原誠二郎 (大学院工学研究科助教授) 化学反応で作ろういろいろな形 化学反応で作ろういろいろな形 ジュニア化学教室, 平成17 年8 月6 日 ジュニア化学教室, 平成17 年8 月6 日 2005 Refereed Japanese Disclose to all
M. Yamamoto; K. Oshima; S. Matsubara M. Yamamoto; K. Oshima; S. Matsubara M. Yamamoto; K. Oshima; S. Matsubara Platinum(IV) oxide catalyzed H-D exchange reactions in arylsilanes Platinum(IV) oxide catalyzed H-D exchange reactions in arylsilanes Platinum(IV) oxide catalyzed H-D exchange reactions in arylsilanes Organic Letters, 6, 26, 5015-5017 Organic Letters, 6, 26, 5015-5017 Organic Letters, 6, 26, 5015-5017 2004/12/23 Refereed English Disclose to all
H. Yoshino; M. Kobata; Y. Yamamoto; K. Oshima; S. Matsubara H. Yoshino; M. Kobata; Y. Yamamoto; K. Oshima; S. Matsubara H. Yoshino; M. Kobata; Y. Yamamoto; K. Oshima; S. Matsubara Wittig type methylenation of ketones with bis(iodozincio)methane and ionic liquid Wittig type methylenation of ketones with bis(iodozincio)methane and ionic liquid Wittig type methylenation of ketones with bis(iodozincio)methane and ionic liquid Chemistry Letters, 33, 9, 1224-1224 Chemistry Letters, 33, 9, 1224-1224 Chemistry Letters, 33, 9, 1224-1224 2004/09/05 Refereed English Disclose to all
K. Nomura; K. Oshima; S. Matsubara K. Nomura; K. Oshima; S. Matsubara K. Nomura; K. Oshima; S. Matsubara Preparation of cis-2-aminocyclopropanol: [2+1] Cycloaddition reaction of bis(iodozincio)methane with α-ketoimine Preparation of cis-2-aminocyclopropanol: [2+1] Cycloaddition reaction of bis(iodozincio)methane with α-ketoimine Preparation of cis-2-aminocyclopropanol: [2+1] Cycloaddition reaction of bis(iodozincio)methane with α-ketoimine Tetrahedron Letters, 45, 31, 5957-5959 Tetrahedron Letters, 45, 31, 5957-5959 Tetrahedron Letters, 45, 31, 5957-5959 2004/07/26 Refereed English Disclose to all
M. Yamamoto; K. Oshima; S. Matsubara M. Yamamoto; K. Oshima; S. Matsubara M. Yamamoto; K. Oshima; S. Matsubara Preparation of deuterium labelled organophosphonium salts (Wittig Salts) under hydrothermal condition catalyzed by molecular sieves Preparation of deuterium labelled organophosphonium salts (Wittig Salts) under hydrothermal condition catalyzed by molecular sieves Preparation of deuterium labelled organophosphonium salts (Wittig Salts) under hydrothermal condition catalyzed by molecular sieves Chemistry Letters, 33, 7, 846-847 Chemistry Letters, 33, 7, 846-847 Chemistry Letters, 33, 7, 846-847 2004/07/05 Refereed English Disclose to all
Y. Yamasaki; T. Hirayama; K. Oshima; S. Matsubara Y. Yamasaki; T. Hirayama; K. Oshima; S. Matsubara Y. Yamasaki; T. Hirayama; K. Oshima; S. Matsubara S<sub>N</sub>2 type hydrolysis of secondary alkyl halides and sulfonates in hydrothermal water S<sub>N</sub>2 type hydrolysis of secondary alkyl halides and sulfonates in hydrothermal water S<sub>N</sub>2 type hydrolysis of secondary alkyl halides and sulfonates in hydrothermal water Chemistry Letters, 33, 7, 864-865 Chemistry Letters, 33, 7, 864-865 Chemistry Letters, 33, 7, 864-865 2004/07/05 Refereed English Disclose to all
H. Yoshino; K. Nomura; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito H. Yoshino; K. Nomura; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito H. Yoshino; K. Nomura; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito A mild ring opening fluorination of epoxide with ionic liquid 1-ethyl-3-methylimidazorium oligo hydrogenfluoride (EMIMF(HF) <sub>2.3</sub>) A mild ring opening fluorination of epoxide with ionic liquid 1-ethyl-3-methylimidazorium oligo hydrogenfluoride (EMIMF(HF) <sub>2.3</sub>) A mild ring opening fluorination of epoxide with ionic liquid 1-ethyl-3-methylimidazorium oligo hydrogenfluoride (EMIMF(HF) <sub>2.3</sub>) Journal of Fluorine Chemistry, 125, 7, 1127-1129 Journal of Fluorine Chemistry, 125, 7, 1127-1129 Journal of Fluorine Chemistry, 125, 7, 1127-1129 2004/07 Refereed English Disclose to all
S. Matsubara; Y. Yokota; K. Oshima S. Matsubara; Y. Yokota; K. Oshima S. Matsubara; Y. Yokota; K. Oshima Palladium-catalyzed H-D exchange reaction under hydrothermal condition Palladium-catalyzed H-D exchange reaction under hydrothermal condition Palladium-catalyzed H-D exchange reaction under hydrothermal condition Chemistry Letters, 33, 3, 294-295 Chemistry Letters, 33, 3, 294-295 Chemistry Letters, 33, 3, 294-295 2004/03/05 Refereed English Disclose to all
H. Yoshino; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito H. Yoshino; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito H. Yoshino; S. Matsubara; K. Oshima; K. Matsumoto; R. Hagiwara; Y. Ito Halofluorination of alkenes with ionic liquid EMIMF(HF)<sub>2.3</sub> Halofluorination of alkenes with ionic liquid EMIMF(HF)<sub>2.3</sub> Halofluorination of alkenes with ionic liquid EMIMF(HF)<sub>2.3</sub> Journal of Fluorine Chemistry, 125, 3, 455-458 Journal of Fluorine Chemistry, 125, 3, 455-458 Journal of Fluorine Chemistry, 125, 3, 455-458 2004/03/01 Refereed English Disclose to all
M. Yamamoto; Y. Yokota; K. Oshima; S. Matsubara M. Yamamoto; Y. Yokota; K. Oshima; S. Matsubara M. Yamamoto; Y. Yokota; K. Oshima; S. Matsubara H-D exchange reaction on benzene ring of polystyrene in hydrothermal deuterium oxide with platinum(IV) oxide catalyst H-D exchange reaction on benzene ring of polystyrene in hydrothermal deuterium oxide with platinum(IV) oxide catalyst H-D exchange reaction on benzene ring of polystyrene in hydrothermal deuterium oxide with platinum(IV) oxide catalyst Chemical Communications, 15, 1714-1715 Chemical Communications, 15, 1714-1715 Chemical Communications, 15, 1714-1715 2004 Refereed English Disclose to all
S. Matsubara; Y. Yokota; K. Oshima S. Matsubara; Y. Yokota; K. Oshima S. Matsubara; Y. Yokota; K. Oshima Palladium-catalyzed decarboxylation and decarbonylation under hydrothermal conditions: Decarboxylative deuteration Palladium-catalyzed decarboxylation and decarbonylation under hydrothermal conditions: Decarboxylative deuteration Palladium-catalyzed decarboxylation and decarbonylation under hydrothermal conditions: Decarboxylative deuteration Organic Letters, 6, 12, 2071-2073 Organic Letters, 6, 12, 2071-2073 Organic Letters, 6, 12, 2071-2073 2004 Refereed English Disclose to all
K. Matsumoto; R. Hagiwara; R. Yoshida; Y. Ito; Z. Mazej; P. Benkič; B. Žemva; O. Tamada; H. Yoshino; S. Matsubara K. Matsumoto; R. Hagiwara; R. Yoshida; Y. Ito; Z. Mazej; P. Benkič; B. Žemva; O. Tamada; H. Yoshino; S. Matsubara K. Matsumoto; R. Hagiwara; R. Yoshida; Y. Ito; Z. Mazej; P. Benkič; B. Žemva; O. Tamada; H. Yoshino; S. Matsubara Syntheses, structures and properties of 1-ethyl-3-methylimidazolium salts of fluorocomplex anions Syntheses, structures and properties of 1-ethyl-3-methylimidazolium salts of fluorocomplex anions Syntheses, structures and properties of 1-ethyl-3-methylimidazolium salts of fluorocomplex anions Dalton Transactions, 1, 144-149 Dalton Transactions, 1, 144-149 Dalton Transactions, 1, 144-149 2004 Refereed English Disclose to all
M. Takahashi; K. Oshima; S. Matsubara M. Takahashi; K. Oshima; S. Matsubara M. Takahashi; K. Oshima; S. Matsubara Hydrogen transfer type oxidation of alcohols by rhodium and ruthenium catalyst under microwave irradiation Hydrogen transfer type oxidation of alcohols by rhodium and ruthenium catalyst under microwave irradiation Hydrogen transfer type oxidation of alcohols by rhodium and ruthenium catalyst under microwave irradiation Tetrahedron Letters, 44, 51, 9201-9203 Tetrahedron Letters, 44, 51, 9201-9203 Tetrahedron Letters, 44, 51, 9201-9203 2003/12/15 Refereed English Disclose to all
S. Matsubara; Y. Kasuga; T. Yasui; M. Yoshioka; B. Yamin; K. Utimoto; K. Oshima S. Matsubara; Y. Kasuga; T. Yasui; M. Yoshioka; B. Yamin; K. Utimoto; K. Oshima S. Matsubara; Y. Kasuga; T. Yasui; M. Yoshioka; B. Yamin; K. Utimoto; K. Oshima Stereocontrolled addition of enolates to chiral 2-acyl-1,3-oxathiane derivatives Stereocontrolled addition of enolates to chiral 2-acyl-1,3-oxathiane derivatives Stereocontrolled addition of enolates to chiral 2-acyl-1,3-oxathiane derivatives Chirality, 15, 1, 38-40 Chirality, 15, 1, 38-40 Chirality, 15, 1, 38-40 2003/01 Refereed English Disclose to all
S. Matsubara; K. Ukai; H. Fushimi; Y. Yokota; H. Yoshino; K. Oshima; K. Omoto; A. Ogawa; Y. Hioki; H. Fujimoto S. Matsubara; K. Ukai; H. Fushimi; Y. Yokota; H. Yoshino; K. Oshima; K. Omoto; A. Ogawa; Y. Hioki; H. Fujimoto S. Matsubara; K. Ukai; H. Fushimi; Y. Yokota; H. Yoshino; K. Oshima; K. Omoto; A. Ogawa; Y. Hioki; H. Fujimoto [2+1] Cycloaddition reaction of bis(iodozincio)methane with 1,2-diketones: Face-to-face complex of bis(iodozincio)methane and 1,2-diketones as a reaction intermediate [2+1] Cycloaddition reaction of bis(iodozincio)methane with 1,2-diketones: Face-to-face complex of bis(iodozincio)methane and 1,2-diketones as a reaction intermediate [2+1] Cycloaddition reaction of bis(iodozincio)methane with 1,2-diketones: Face-to-face complex of bis(iodozincio)methane and 1,2-diketones as a reaction intermediate Tetrahedron, 58, 41, 8255-8262 Tetrahedron, 58, 41, 8255-8262 Tetrahedron, 58, 41, 8255-8262 2002/10/07 Refereed English Disclose to all
S. Matsubara; H. Yamamoto; K. Oshima; E. Mouri; H. Matsuoka S. Matsubara; H. Yamamoto; K. Oshima; E. Mouri; H. Matsuoka S. Matsubara; H. Yamamoto; K. Oshima; E. Mouri; H. Matsuoka Fabrication of nano-structure by Diels-Alder reaction Fabrication of nano-structure by Diels-Alder reaction Fabrication of nano-structure by Diels-Alder reaction Chemistry Letters, 9, 886-887 Chemistry Letters, 9, 886-887 Chemistry Letters, 9, 886-887 2002/09/05 Refereed English Disclose to all
H. Takahashi; E. Matsubara; R.V. Belosludov; S. Matsubara; N. Sato; A. Muramatsu; Y. Kawazoe; K. Tohji H. Takahashi; E. Matsubara; R.V. Belosludov; S. Matsubara; N. Sato; A. Muramatsu; Y. Kawazoe; K. Tohji H. Takahashi; E. Matsubara; R.V. Belosludov; S. Matsubara; N. Sato; A. Muramatsu; Y. Kawazoe; K. Tohji Fullerene and sulfur compounds Fullerene and sulfur compounds Fullerene and sulfur compounds Materials Transactions, 43, 7, 1530-1532 Materials Transactions, 43, 7, 1530-1532 Materials Transactions, 43, 7, 1530-1532 2002/07 Refereed English Disclose to all
S. Matsubara; K. Oshima; E. Matsubara S. Matsubara; K. Oshima; E. Matsubara Ingredients of the soup in the chemist\\'s cauldron: Structured analysis of organometallics in the solution by X-ray Ingredients of the soup in the chemist\\'s cauldron: Structured analysis of organometallics in the solution by X-ray Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 60, 4, 383-388 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 60, 4, 383-388 , 60, 4, 383-388 2002/04 Refereed Japanese Disclose to all
T. Tsuji; S.-i. Usugi; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima T. Tsuji; S.-i. Usugi; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima T. Tsuji; S.-i. Usugi; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima Allylation of carbonyl compounds with allylic gallium reagents Allylation of carbonyl compounds with allylic gallium reagents Allylation of carbonyl compounds with allylic gallium reagents Chemistry Letters, 1, 2-3 Chemistry Letters, 1, 2-3 Chemistry Letters, 1, 2-3 2002/01/05 Refereed English Disclose to all
S. Matsubara; H. Yamamoto; K. Oshima S. Matsubara; H. Yamamoto; K. Oshima S. Matsubara; H. Yamamoto; K. Oshima Stereoselective pinacol-type rearrangement of 2,3-epoxy alcohols with retention of configuration mediated by bis(iodozincio)methane Stereoselective pinacol-type rearrangement of 2,3-epoxy alcohols with retention of configuration mediated by bis(iodozincio)methane Stereoselective pinacol-type rearrangement of 2,3-epoxy alcohols with retention of configuration mediated by bis(iodozincio)methane Angewandte Chemie - International Edition, 41, 15, 2837-+ Angewandte Chemie - International Edition, 41, 15, 2837-+ Angewandte Chemie - International Edition, 41, 15, 2837-+ 2002 Refereed English Disclose to all
H. Takahashi; E. Matsubara; M. Shiro; S. Matsubara; N. Sato; A. Muramatsu; K. Tohji H. Takahashi; E. Matsubara; M. Shiro; S. Matsubara; N. Sato; A. Muramatsu; K. Tohji H. Takahashi; E. Matsubara; M. Shiro; S. Matsubara; N. Sato; A. Muramatsu; K. Tohji Co-deposition of fullerenes and sulfur from diluted solution Co-deposition of fullerenes and sulfur from diluted solution Co-deposition of fullerenes and sulfur from diluted solution Fullerenes Nanotubes and Carbon Nanostructures, 10, 3, 217-226 Fullerenes Nanotubes and Carbon Nanostructures, 10, 3, 217-226 Fullerenes Nanotubes and Carbon Nanostructures, 10, 3, 217-226 2002 Refereed English Disclose to all
K. Fujita; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima K. Fujita; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima K. Fujita; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima Conversion of acid chloride into homoallylic alcohol via allylic C-H bond activation of alkene with a zirconocene complex [16] Conversion of acid chloride into homoallylic alcohol via allylic C-H bond activation of alkene with a zirconocene complex [16] Conversion of acid chloride into homoallylic alcohol via allylic C-H bond activation of alkene with a zirconocene complex [16] Journal of the American Chemical Society, 123, 48, 12115-12116 Journal of the American Chemical Society, 123, 48, 12115-12116 Journal of the American Chemical Society, 123, 48, 12115-12116 2001/12/05 Refereed English Disclose to all
S. Matsubara; T. Ikeda; K. Oshima; K. Utimoto S. Matsubara; T. Ikeda; K. Oshima; K. Utimoto S. Matsubara; T. Ikeda; K. Oshima; K. Utimoto Preparation of organoytterbium reagent from ytterbium trichloride and organomagnesium Preparation of organoytterbium reagent from ytterbium trichloride and organomagnesium Preparation of organoytterbium reagent from ytterbium trichloride and organomagnesium Chemistry Letters, 12, 1226-1227 Chemistry Letters, 12, 1226-1227 Chemistry Letters, 12, 1226-1227 2001/12/05 Refereed English Disclose to all
H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima; K. Omoto; H. Fujimoto H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima; K. Omoto; H. Fujimoto H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima; K. Omoto; H. Fujimoto Triethylborane-induced bromine atom-transfer radical addition in aqueous media: Study of the solvent effect on radical addition reactions Triethylborane-induced bromine atom-transfer radical addition in aqueous media: Study of the solvent effect on radical addition reactions Triethylborane-induced bromine atom-transfer radical addition in aqueous media: Study of the solvent effect on radical addition reactions Journal of Organic Chemistry, 66, 23, 7776-7785 Journal of Organic Chemistry, 66, 23, 7776-7785 Journal of Organic Chemistry, 66, 23, 7776-7785 2001/11/16 Refereed English Disclose to all
H. Kinoshita; T. Nakamura; H. Kakiya; H. Shinokubo; S. Matsubara; K. Oshima H. Kinoshita; T. Nakamura; H. Kakiya; H. Shinokubo; S. Matsubara; K. Oshima H. Kinoshita; T. Nakamura; H. Kakiya; H. Shinokubo; S. Matsubara; K. Oshima Remarkable rate acceleration of Pd(0)-catalyzed hydrogermylation of alkynes and dienes in water Remarkable rate acceleration of Pd(0)-catalyzed hydrogermylation of alkynes and dienes in water Remarkable rate acceleration of Pd(0)-catalyzed hydrogermylation of alkynes and dienes in water Organic Letters, 3, 16, 2521-2524 Organic Letters, 3, 16, 2521-2524 Organic Letters, 3, 16, 2521-2524 2001/08/09 Refereed English Disclose to all
S. Tanaka; T. Nakamura; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima S. Tanaka; T. Nakamura; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima S. Tanaka; T. Nakamura; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima Radical addition of triphenylgermane to vinyloxiranes: Its application to synthesis of 4-vinyltetrahydro-2-furanones Radical addition of triphenylgermane to vinyloxiranes: Its application to synthesis of 4-vinyltetrahydro-2-furanones Radical addition of triphenylgermane to vinyloxiranes: Its application to synthesis of 4-vinyltetrahydro-2-furanones Synlett, 8, 1278-1280 Synlett, 8, 1278-1280 Synlett, 8, 1278-1280 2001/08 Refereed English Disclose to all
K. Takami; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima K. Takami; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima K. Takami; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima Palladium-Catalyzed Cross-Coupling Reaction of Organoindiums with Aryl Halides in Aqueous Media Palladium-Catalyzed Cross-Coupling Reaction of Organoindiums with Aryl Halides in Aqueous Media Palladium-Catalyzed Cross-Coupling Reaction of Organoindiums with Aryl Halides in Aqueous Media Organic Letters, 3, 13, 1997-1999 Organic Letters, 3, 13, 1997-1999 Organic Letters, 3, 13, 1997-1999 2001/06/28 Refereed English Disclose to all
S. Mikami; K. Fujita; T. Nakamura; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima S. Mikami; K. Fujita; T. Nakamura; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima S. Mikami; K. Fujita; T. Nakamura; H. Yorimitsu; H. Shinokubo; S. Matsubara; K. Oshima Triethylborane-induced radical reactions with gallium hydride reagent HGaCl<sub>2</sub> Triethylborane-induced radical reactions with gallium hydride reagent HGaCl<sub>2</sub> Triethylborane-induced radical reactions with gallium hydride reagent HGaCl<sub>2</sub> Organic Letters, 3, 12, 1853-1855 Organic Letters, 3, 12, 1853-1855 Organic Letters, 3, 12, 1853-1855 2001/06/14 Refereed English Disclose to all
K. Ukai; D. Arioka; H. Yoshino; H. Fushimi; K. Oshima; K. Utimoto; S. Matsubara K. Ukai; D. Arioka; H. Yoshino; H. Fushimi; K. Oshima; K. Utimoto; S. Matsubara K. Ukai; D. Arioka; H. Yoshino; H. Fushimi; K. Oshima; K. Utimoto; S. Matsubara α-oxygen-atom induced methylenation of ketones by CH<sub>2</sub>(ZnI)<sub>2</sub> α-oxygen-atom induced methylenation of ketones by CH<sub>2</sub>(ZnI)<sub>2</sub> α-oxygen-atom induced methylenation of ketones by CH<sub>2</sub>(ZnI)<sub>2</sub> Synlett, 4, 513-514 Synlett, 4, 513-514 Synlett, 4, 513-514 2001/04 Refereed English Disclose to all
K. Utimoto; Y. Otake; H. Yoshino; E. Kuwahara; K. Oshima; S. Matsubara K. Utimoto; Y. Otake; H. Yoshino; E. Kuwahara; K. Oshima; S. Matsubara K. Utimoto; Y. Otake; H. Yoshino; E. Kuwahara; K. Oshima; S. Matsubara The rate enhancement effect of protodesilylation of arylsilane derivatives The rate enhancement effect of protodesilylation of arylsilane derivatives The rate enhancement effect of protodesilylation of arylsilane derivatives Bulletin of the Chemical Society of Japan, 74, 4, 753-754 Bulletin of the Chemical Society of Japan, 74, 4, 753-754 Bulletin of the Chemical Society of Japan, 74, 4, 753-754 2001/04 Refereed English Disclose to all
Y. Hashimoto; U. Mizuno; H. Matsuoka; T. Miyahara; M. Takakura; M. Yoshimoto; K. Oshima; K. Utimoto; S. Matsubara Y. Hashimoto; U. Mizuno; H. Matsuoka; T. Miyahara; M. Takakura; M. Yoshimoto; K. Oshima; K. Utimoto; S. Matsubara Y. Hashimoto; U. Mizuno; H. Matsuoka; T. Miyahara; M. Takakura; M. Yoshimoto; K. Oshima; K. Utimoto; S. Matsubara Structural studies of the low-valent titanium "Solution": What goes on in the pinacol coupling reaction? [3] Structural studies of the low-valent titanium "Solution": What goes on in the pinacol coupling reaction? [3] Structural studies of the low-valent titanium "Solution": What goes on in the pinacol coupling reaction? [3] Journal of the American Chemical Society, 123, 7, 1503-1504 Journal of the American Chemical Society, 123, 7, 1503-1504 Journal of the American Chemical Society, 123, 7, 1503-1504 2001/02/21 Refereed English Disclose to all
Takami, K; Yorimitsu, H; Shinokubo, H; Matsubara, S; Oshima, K Takami, K; Yorimitsu, H; Shinokubo, H; Matsubara, S; Oshima, K Takami, K; Yorimitsu, H; Shinokubo, H; Matsubara, S; Oshima, K Iodotrimethylsilane-induced cyclization of 6-alkynal acetals Iodotrimethylsilane-induced cyclization of 6-alkynal acetals Iodotrimethylsilane-induced cyclization of 6-alkynal acetals SYNLETT, 2, 293-295 SYNLETT, 2, 293-295 SYNLETT, 2, 293-295 2001/02 Refereed English Disclose to all
S. Matsubara; K. Oshima; K. Utimoto S. Matsubara; K. Oshima; K. Utimoto S. Matsubara; K. Oshima; K. Utimoto Bis(iodozincio)methane - Preparation, structure, and reaction Bis(iodozincio)methane - Preparation, structure, and reaction Bis(iodozincio)methane - Preparation, structure, and reaction Journal of Organometallic Chemistry, 617, 1, 39-46 Journal of Organometallic Chemistry, 617, 1, 39-46 Journal of Organometallic Chemistry, 617, 1, 39-46 2001/01/15 Refereed English Disclose to all
K. Ukai; K. Oshima; S. Matsubara K. Ukai; K. Oshima; S. Matsubara K. Ukai; K. Oshima; S. Matsubara Preparation of cyclopropanediol: Novel [2 + 1] cycloaddition reaction of bis(iodozincio)methane with 1,2-diketones [27] Preparation of cyclopropanediol: Novel [2 + 1] cycloaddition reaction of bis(iodozincio)methane with 1,2-diketones [27] Preparation of cyclopropanediol: Novel [2 + 1] cycloaddition reaction of bis(iodozincio)methane with 1,2-diketones [27] Journal of the American Chemical Society, 122, 48, 12047-12048 Journal of the American Chemical Society, 122, 48, 12047-12048 Journal of the American Chemical Society, 122, 48, 12047-12048 2000/12/06 Refereed English Disclose to all
Matsubara, S; Yamamoto, H; Arioka, D; Utimoto, K; Oshima, K Matsubara, S; Yamamoto, H; Arioka, D; Utimoto, K; Oshima, K Matsubara, S; Yamamoto, H; Arioka, D; Utimoto, K; Oshima, K Diastereoselective 1,4-addition reactions of bis(iodozincio)ethane to alpha,beta-unsaturated ketones Diastereoselective 1,4-addition reactions of bis(iodozincio)ethane to alpha,beta-unsaturated ketones Diastereoselective 1,4-addition reactions of bis(iodozincio)ethane to alpha,beta-unsaturated ketones SYNLETT, 8, 1202-1204 SYNLETT, 8, 1202-1204 SYNLETT, 8, 1202-1204 2000/08 Refereed English Disclose to all
S. Matsubara; N. Toda; M. Kobata; K. Utimoto S. Matsubara; N. Toda; M. Kobata; K. Utimoto S. Matsubara; N. Toda; M. Kobata; K. Utimoto Preparation of chiral organozinc compounds via desymmetrization of gem- dizincioethane Preparation of chiral organozinc compounds via desymmetrization of gem- dizincioethane Preparation of chiral organozinc compounds via desymmetrization of gem- dizincioethane Synlett, 7, 987-988 Synlett, 7, 987-988 Synlett, 7, 987-988 2000/07 Refereed English Disclose to all
S. Matsubara; K. Ukai; N. Toda; K. Utimoto; K. Oshima S. Matsubara; K. Ukai; N. Toda; K. Utimoto; K. Oshima S. Matsubara; K. Ukai; N. Toda; K. Utimoto; K. Oshima Preparation of 1,2-drones and 1,3-dienes assembling three units Preparation of 1,2-drones and 1,3-dienes assembling three units Preparation of 1,2-drones and 1,3-dienes assembling three units Synlett, 7, 995-996 Synlett, 7, 995-996 Synlett, 7, 995-996 2000/07 Refereed English Disclose to all
S. Matsubara; H. Yoshino; K. Utimoto; K. Oshima S. Matsubara; H. Yoshino; K. Utimoto; K. Oshima S. Matsubara; H. Yoshino; K. Utimoto; K. Oshima Preparation of germyl-substituted dizinciomethanes and their reactions with electrophiles Preparation of germyl-substituted dizinciomethanes and their reactions with electrophiles Preparation of germyl-substituted dizinciomethanes and their reactions with electrophiles Synlett, 4, 495-496 Synlett, 4, 495-496 Synlett, 4, 495-496 2000/04 Refereed English Disclose to all
S. Matsubara S. Matsubara S. Matsubara The reaction using gem-dizinc compounds: Structure and reactivity The reaction using gem-dizinc compounds: Structure and reactivity The reaction using gem-dizinc compounds: Structure and reactivity Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 58, 2, 108-113 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 58, 2, 108-113 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 58, 2, 108-113 2000/02 Refereed English Disclose to all
S. Matsubara; D. Arioka; K. Utimoto S. Matsubara; D. Arioka; K. Utimoto S. Matsubara; D. Arioka; K. Utimoto 1,4-Addition reactions of bis(iodozincio)methane with α,β-unsaturated ketones 1,4-Addition reactions of bis(iodozincio)methane with α,β-unsaturated ketones 1,4-Addition reactions of bis(iodozincio)methane with α,β-unsaturated ketones Synlett, 8, 1253-1254 Synlett, 8, 1253-1254 Synlett, 8, 1253-1254 1999 Refereed English Disclose to all
S. Matsubara; Y. Hashimoto; T. Okano; K. Utimoto S. Matsubara; Y. Hashimoto; T. Okano; K. Utimoto S. Matsubara; Y. Hashimoto; T. Okano; K. Utimoto Pinacol coupling of benzaldehyde with TiCl<sub>2</sub>-amine Pinacol coupling of benzaldehyde with TiCl<sub>2</sub>-amine Pinacol coupling of benzaldehyde with TiCl<sub>2</sub>-amine Synlett, 9, 1411-1412 Synlett, 9, 1411-1412 Synlett, 9, 1411-1412 1999 Refereed English Disclose to all
S. Matsubara; Y. Yamamoto; K. Utimoto S. Matsubara; Y. Yamamoto; K. Utimoto S. Matsubara; Y. Yamamoto; K. Utimoto Structure and reactivity of bis(iodozincio)methane in tetrahydrothiophene Structure and reactivity of bis(iodozincio)methane in tetrahydrothiophene Structure and reactivity of bis(iodozincio)methane in tetrahydrothiophene Synlett, 9, 1471-1473 Synlett, 9, 1471-1473 Synlett, 9, 1471-1473 1999 Refereed English Disclose to all
S. Matsubara; K. Ukai; T. Mizuno; K. Utimoto S. Matsubara; K. Ukai; T. Mizuno; K. Utimoto S. Matsubara; K. Ukai; T. Mizuno; K. Utimoto Methylenation of esters with bis(iodozincio)methane-TiCl<sub>2</sub>-TMEDA system Methylenation of esters with bis(iodozincio)methane-TiCl<sub>2</sub>-TMEDA system Methylenation of esters with bis(iodozincio)methane-TiCl<sub>2</sub>-TMEDA system Chemistry Letters, 8, 825-826 Chemistry Letters, 8, 825-826 Chemistry Letters, 8, 825-826 1999 Refereed English Disclose to all
S. Matsubara; Y. Otake; Y. Hashimoto; K. Utimoto S. Matsubara; Y. Otake; Y. Hashimoto; K. Utimoto S. Matsubara; Y. Otake; Y. Hashimoto; K. Utimoto Preparation of dialkoxyborylbis(bromozincio)methane and its reaction with electrophiles Preparation of dialkoxyborylbis(bromozincio)methane and its reaction with electrophiles Preparation of dialkoxyborylbis(bromozincio)methane and its reaction with electrophiles Chemistry Letters, 8, 747-748 Chemistry Letters, 8, 747-748 Chemistry Letters, 8, 747-748 1999 Refereed English Disclose to all
S. Matsubara; T. Mizuno; T. Otake; M. Kobata; K. Utimoto; K. Takai S. Matsubara; T. Mizuno; T. Otake; M. Kobata; K. Utimoto; K. Takai S. Matsubara; T. Mizuno; T. Otake; M. Kobata; K. Utimoto; K. Takai Alkylidenation of carbonyl compounds with gem-dizincioalkanes mediated with titanium dichloride Alkylidenation of carbonyl compounds with gem-dizincioalkanes mediated with titanium dichloride Alkylidenation of carbonyl compounds with gem-dizincioalkanes mediated with titanium dichloride Synlett, 12, 1369-1371 Synlett, 12, 1369-1371 Synlett, 12, 1369-1371 1998 Refereed English Disclose to all
S. Matsubara; M. Sugihara; K. Utimoto S. Matsubara; M. Sugihara; K. Utimoto S. Matsubara; M. Sugihara; K. Utimoto Methylenation of carbonyl compounds by means of Nysted reagent Methylenation of carbonyl compounds by means of Nysted reagent Methylenation of carbonyl compounds by means of Nysted reagent Synlett, 3, 313-315 Synlett, 3, 313-315 Synlett, 3, 313-315 1998 Refereed English Disclose to all
S. Matsubara; K. Kawamoto; K. Utimoto S. Matsubara; K. Kawamoto; K. Utimoto S. Matsubara; K. Kawamoto; K. Utimoto Preparation of 1,3-diketones by the reaction of bis(iodozincio)methene with acyl cyanides or palladium-catalyzed reaction with acyl chlorides Preparation of 1,3-diketones by the reaction of bis(iodozincio)methene with acyl cyanides or palladium-catalyzed reaction with acyl chlorides Preparation of 1,3-diketones by the reaction of bis(iodozincio)methene with acyl cyanides or palladium-catalyzed reaction with acyl chlorides Synlett, 3, 267-268 Synlett, 3, 267-268 Synlett, 3, 267-268 1998 Refereed English Disclose to all
K. Utimoto; N. Toda; T. Mizuno; M. Kobata; S. Matsubara K. Utimoto; N. Toda; T. Mizuno; M. Kobata; S. Matsubara K. Utimoto; N. Toda; T. Mizuno; M. Kobata; S. Matsubara Stepwise reaction of bis(iodozincio)methane with two different electrophiles Stepwise reaction of bis(iodozincio)methane with two different electrophiles Stepwise reaction of bis(iodozincio)methane with two different electrophiles Angewandte Chemie - International Edition in English, 36, 24, 2804-2805 Angewandte Chemie - International Edition in English, 36, 24, 2804-2805 Angewandte Chemie - International Edition in English, 36, 24, 2804-2805 1998 Refereed English Disclose to all
K. Utimoto; S. Matsubara K. Utimoto; S. Matsubara K. Utimoto; S. Matsubara Samarium Diiodide-Mediated Reaction Of Organic Halides With Carbonyl Compounds Samarium Diiodide-Mediated Reaction Of Organic Halides With Carbonyl Compounds Samarium Diiodide-Mediated Reaction Of Organic Halides With Carbonyl Compounds Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 56, 11, 908-918 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 56, 11, 908-918 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 56, 11, 908-918 1998 Refereed English Disclose to all
Y. Kasuga; S. Matsubara; K. Utimoto Y. Kasuga; S. Matsubara; K. Utimoto Y. Kasuga; S. Matsubara; K. Utimoto Stereoselective reaction with configurationally stable α-phenylthioalkylsamarium compounds Stereoselective reaction with configurationally stable α-phenylthioalkylsamarium compounds Stereoselective reaction with configurationally stable α-phenylthioalkylsamarium compounds Synlett, 8, 840-842 Synlett, 8, 840-842 Synlett, 8, 840-842 1998 Refereed English Disclose to all
S. Matsubara; M. Yoshioka; K. Utimoto S. Matsubara; M. Yoshioka; K. Utimoto S. Matsubara; M. Yoshioka; K. Utimoto A samarium-mediated, highly stereoselective reaction of 1,1-dihaloalkanes with aldehydes: Generation of a chiral α-iodoethyl building block from achiral 1,1-diiodoethane A samarium-mediated, highly stereoselective reaction of 1,1-dihaloalkanes with aldehydes: Generation of a chiral α-iodoethyl building block from achiral 1,1-diiodoethane A samarium-mediated, highly stereoselective reaction of 1,1-dihaloalkanes with aldehydes: Generation of a chiral α-iodoethyl building block from achiral 1,1-diiodoethane Angewandte Chemie - International Edition in English, 36, 6, 617-618 Angewandte Chemie - International Edition in English, 36, 6, 617-618 Angewandte Chemie - International Edition in English, 36, 6, 617-618 1997 Refereed English Disclose to all
N. Nakanishi; S. Matsubara; K. Utimoto; S. Kozima; R. Yamaguchi N. Nakanishi; S. Matsubara; K. Utimoto; S. Kozima; R. Yamaguchi N. Nakanishi; S. Matsubara; K. Utimoto; S. Kozima; R. Yamaguchi Regioselective ε-alkylation of 5-acetoxy-1,3-alkadienes by organocopper-magnesium reagents Regioselective ε-alkylation of 5-acetoxy-1,3-alkadienes by organocopper-magnesium reagents Regioselective ε-alkylation of 5-acetoxy-1,3-alkadienes by organocopper-magnesium reagents Journal of Organic Chemistry, 56, 10, 3278-3283 Journal of Organic Chemistry, 56, 10, 3278-3283 Journal of Organic Chemistry, 56, 10, 3278-3283 1991 Refereed English Disclose to all
Y. Fukuda; S. Matsubara; K. Utimoto Y. Fukuda; S. Matsubara; K. Utimoto Y. Fukuda; S. Matsubara; K. Utimoto Palladium-catalyzed intramolecular addition of amines to acetylenes. Synthesis of cyclic imines Palladium-catalyzed intramolecular addition of amines to acetylenes. Synthesis of cyclic imines Palladium-catalyzed intramolecular addition of amines to acetylenes. Synthesis of cyclic imines Journal of Organic Chemistry, 56, 20, 5812-5816 Journal of Organic Chemistry, 56, 20, 5812-5816 Journal of Organic Chemistry, 56, 20, 5812-5816 1991 Refereed English Disclose to all
S. Matsubara; T. Kodama; K. Utimoto S. Matsubara; T. Kodama; K. Utimoto S. Matsubara; T. Kodama; K. Utimoto Yb(CN)<sub>3</sub>-catalyzed reaction of aziridines with cyanotrimethylsilane. A facile synthesis of optically pure β-amino nitriles Yb(CN)<sub>3</sub>-catalyzed reaction of aziridines with cyanotrimethylsilane. A facile synthesis of optically pure β-amino nitriles Yb(CN)<sub>3</sub>-catalyzed reaction of aziridines with cyanotrimethylsilane. A facile synthesis of optically pure β-amino nitriles Tetrahedron Letters, 31, 44, 6379-6380 Tetrahedron Letters, 31, 44, 6379-6380 Tetrahedron Letters, 31, 44, 6379-6380 1990 Refereed English Disclose to all
S. Matsubara; H. Onishi; K. Utimoto S. Matsubara; H. Onishi; K. Utimoto S. Matsubara; H. Onishi; K. Utimoto Reaction of cyanotrimethylsilane with oxiranes under Yb(CN)<sub>3</sub> catalysis Reaction of cyanotrimethylsilane with oxiranes under Yb(CN)<sub>3</sub> catalysis Reaction of cyanotrimethylsilane with oxiranes under Yb(CN)<sub>3</sub> catalysis Tetrahedron Letters, 31, 43, 6209-6212 Tetrahedron Letters, 31, 43, 6209-6212 Tetrahedron Letters, 31, 43, 6209-6212 1990 Refereed English Disclose to all
B.M. Trost; S. Matsubara; J.J. Caringi B.M. Trost; S. Matsubara; J.J. Caringi B.M. Trost; S. Matsubara; J.J. Caringi Cycloisomerization of α,ω-diynes to macrocycles Cycloisomerization of α,ω-diynes to macrocycles Cycloisomerization of α,ω-diynes to macrocycles Journal of the American Chemical Society, 111, 23, 8745-8746 Journal of the American Chemical Society, 111, 23, 8745-8746 Journal of the American Chemical Society, 111, 23, 8745-8746 1989 Refereed English Disclose to all
K. Iritani; S. Matsubara; K. Utimoto K. Iritani; S. Matsubara; K. Utimoto K. Iritani; S. Matsubara; K. Utimoto Palladium catalyzed reaction of 2-alkynylanilines with allyl chlorides. Formation of 3-allylindoles Palladium catalyzed reaction of 2-alkynylanilines with allyl chlorides. Formation of 3-allylindoles Palladium catalyzed reaction of 2-alkynylanilines with allyl chlorides. Formation of 3-allylindoles Tetrahedron Letters, 29, 15, 1799-1802 Tetrahedron Letters, 29, 15, 1799-1802 Tetrahedron Letters, 29, 15, 1799-1802 1988 Refereed English Disclose to all
T. Hamatani; S. Matsubara; H. Matsuda; M. Schlosser T. Hamatani; S. Matsubara; H. Matsuda; M. Schlosser T. Hamatani; S. Matsubara; H. Matsuda; M. Schlosser A stereocontrolled access to vicinal difluoroalkanes A stereocontrolled access to vicinal difluoroalkanes A stereocontrolled access to vicinal difluoroalkanes Tetrahedron, 44, 10, 2875-2881 Tetrahedron, 44, 10, 2875-2881 Tetrahedron, 44, 10, 2875-2881 1988 Refereed English Disclose to all
S. Matsubara; H. Matsuda; T. Hamatani; M. Schlosser S. Matsubara; H. Matsuda; T. Hamatani; M. Schlosser S. Matsubara; H. Matsuda; T. Hamatani; M. Schlosser Base-promoted elimination of hydrogen fluoride from alkyl fluorides : Reactivity and stereochemistry Base-promoted elimination of hydrogen fluoride from alkyl fluorides : Reactivity and stereochemistry Base-promoted elimination of hydrogen fluoride from alkyl fluorides : Reactivity and stereochemistry Tetrahedron, 44, 10, 2855-2863 Tetrahedron, 44, 10, 2855-2863 Tetrahedron, 44, 10, 2855-2863 1988 Refereed English Disclose to all
H. Shiragami; T. Kawamoto; K. Imi; S. Matsubara; K. Utimoto; H. Nozaki H. Shiragami; T. Kawamoto; K. Imi; S. Matsubara; K. Utimoto; H. Nozaki H. Shiragami; T. Kawamoto; K. Imi; S. Matsubara; K. Utimoto; H. Nozaki Novel rearrangement of chloromethylvinylsilanes into allylsilanes. Stereoselective synthesis of metallated allylsilanes from 1-alkynes Novel rearrangement of chloromethylvinylsilanes into allylsilanes. Stereoselective synthesis of metallated allylsilanes from 1-alkynes Novel rearrangement of chloromethylvinylsilanes into allylsilanes. Stereoselective synthesis of metallated allylsilanes from 1-alkynes Tetrahedron, 44, 13, 4009-4022 Tetrahedron, 44, 13, 4009-4022 Tetrahedron, 44, 13, 4009-4022 1988 Refereed English Disclose to all
K. Fugami; J.-i. Hibino; S. Nakatsukasa; S. Matsubara; K. Oshima; K. Utimoto; H. Nozaki K. Fugami; J.-i. Hibino; S. Nakatsukasa; S. Matsubara; K. Oshima; K. Utimoto; H. Nozaki K. Fugami; J.-i. Hibino; S. Nakatsukasa; S. Matsubara; K. Oshima; K. Utimoto; H. Nozaki Organic synthesis with reagents derived from 3R<sub>3</sub>SiMgMe and MnCl<sub>2</sub> Organic synthesis with reagents derived from 3R<sub>3</sub>SiMgMe and MnCl<sub>2</sub> Organic synthesis with reagents derived from 3R<sub>3</sub>SiMgMe and MnCl<sub>2</sub> Tetrahedron, 44, 13, 4277-4292 Tetrahedron, 44, 13, 4277-4292 Tetrahedron, 44, 13, 4277-4292 1988 Refereed English Disclose to all
S. Matsubara; M. Mitani; K. Utimoto S. Matsubara; M. Mitani; K. Utimoto S. Matsubara; M. Mitani; K. Utimoto A facile preparation of 1-perflouroalkylalkenes and alkynes. Palladium catalyzed reaction of perfluoroalkyl iodides with organotin compounds A facile preparation of 1-perflouroalkylalkenes and alkynes. Palladium catalyzed reaction of perfluoroalkyl iodides with organotin compounds A facile preparation of 1-perflouroalkylalkenes and alkynes. Palladium catalyzed reaction of perfluoroalkyl iodides with organotin compounds Tetrahedron Letters, 28, 47, 5857-5860 Tetrahedron Letters, 28, 47, 5857-5860 Tetrahedron Letters, 28, 47, 5857-5860 1987 Refereed English Disclose to all
T. Ishii; N. Kawamura; S. Matsubara; K. Utimoto; S. Kozima; T. Hitomi T. Ishii; N. Kawamura; S. Matsubara; K. Utimoto; S. Kozima; T. Hitomi T. Ishii; N. Kawamura; S. Matsubara; K. Utimoto; S. Kozima; T. Hitomi A facile stereoselective synthesis of internal conjugated (E,E)-dienes including 2,4-alkadienylamines, -silanes, and -stannanes A facile stereoselective synthesis of internal conjugated (E,E)-dienes including 2,4-alkadienylamines, -silanes, and -stannanes A facile stereoselective synthesis of internal conjugated (E,E)-dienes including 2,4-alkadienylamines, -silanes, and -stannanes Journal of Organic Chemistry, 52, 19, 4416-4418 Journal of Organic Chemistry, 52, 19, 4416-4418 Journal of Organic Chemistry, 52, 19, 4416-4418 1987 Refereed English Disclose to all
T. Nonaka; Y. Okuda; S. Matsubara; K. Oshima; K. Utimoto; H. Nozaki T. Nonaka; Y. Okuda; S. Matsubara; K. Oshima; K. Utimoto; H. Nozaki T. Nonaka; Y. Okuda; S. Matsubara; K. Oshima; K. Utimoto; H. Nozaki New synthetic reactions with (Ph<sub>3</sub>Sn)<sub>2</sub>Zn·TMEDA complex. Regio- and stereoselective synthesis of vinylstannanes New synthetic reactions with (Ph<sub>3</sub>Sn)<sub>2</sub>Zn·TMEDA complex. Regio- and stereoselective synthesis of vinylstannanes New synthetic reactions with (Ph<sub>3</sub>Sn)<sub>2</sub>Zn·TMEDA complex. Regio- and stereoselective synthesis of vinylstannanes Journal of Organic Chemistry, 51, 24, 4716-4718 Journal of Organic Chemistry, 51, 24, 4716-4718 Journal of Organic Chemistry, 51, 24, 4716-4718 1986 Refereed English Disclose to all
S. Matsubara; J.-I. Hibino; Y. Morizawa; K. Oshima; H. Nozaki S. Matsubara; J.-I. Hibino; Y. Morizawa; K. Oshima; H. Nozaki S. Matsubara; J.-I. Hibino; Y. Morizawa; K. Oshima; H. Nozaki Regio- and stereo-selective synthesis of vinylstannanes. Transition-metal catalyzed stannylmetalation of acetylenes and conversion of enol triflates and vinyl iodides into vinylstannanes Regio- and stereo-selective synthesis of vinylstannanes. Transition-metal catalyzed stannylmetalation of acetylenes and conversion of enol triflates and vinyl iodides into vinylstannanes Regio- and stereo-selective synthesis of vinylstannanes. Transition-metal catalyzed stannylmetalation of acetylenes and conversion of enol triflates and vinyl iodides into vinylstannanes Journal of Organometallic Chemistry, 285, 1-3, 163-172 Journal of Organometallic Chemistry, 285, 1-3, 163-172 Journal of Organometallic Chemistry, 285, 1-3, 163-172 1985 Refereed English Disclose to all
Seijiro Matsubara; Takashi Okazoe; Koichiro Oshima; Kazuhiko Takai; Hitosi Nozaki Seijiro Matsubara; Takashi Okazoe; Koichiro Oshima; Kazuhiko Takai; Hitosi Nozaki Seijiro Matsubara; Takashi Okazoe; Koichiro Oshima; Kazuhiko Takai; Hitosi Nozaki ISOMERIZATION OF ALLYLIC ALCOHOLS CATALYZED BY VANADIUM OR MOLYBDENUM COMPLEXES. ISOMERIZATION OF ALLYLIC ALCOHOLS CATALYZED BY VANADIUM OR MOLYBDENUM COMPLEXES. ISOMERIZATION OF ALLYLIC ALCOHOLS CATALYZED BY VANADIUM OR MOLYBDENUM COMPLEXES. Bulletin of the Chemical Society of Japan, 58, 3, 844-849 Bulletin of the Chemical Society of Japan, 58, 3, 844-849 Bulletin of the Chemical Society of Japan, 58, 3, 844-849 1985 Refereed English Disclose to all
J.-I. Hibino; S. Nakatsukasa; K. Fugami; S. Matsubara; K. Oshima; H. Nozaki J.-I. Hibino; S. Nakatsukasa; K. Fugami; S. Matsubara; K. Oshima; H. Nozaki J.-I. Hibino; S. Nakatsukasa; K. Fugami; S. Matsubara; K. Oshima; H. Nozaki Disilylation of acetylenes with Si-Mn reagent Disilylation of acetylenes with Si-Mn reagent Disilylation of acetylenes with Si-Mn reagent Journal of the American Chemical Society, 107, 22, 6416-6417 Journal of the American Chemical Society, 107, 22, 6416-6417 Journal of the American Chemical Society, 107, 22, 6416-6417 1985 Refereed English Disclose to all
J.-i. Hibino; S. Matsubara; Y. Morizawa; K. Oshima; H. Nozaki J.-i. Hibino; S. Matsubara; Y. Morizawa; K. Oshima; H. Nozaki J.-i. Hibino; S. Matsubara; Y. Morizawa; K. Oshima; H. Nozaki Regioselective stannylmetalation of acetylenes in the presence of transition-metal catalyst Regioselective stannylmetalation of acetylenes in the presence of transition-metal catalyst Regioselective stannylmetalation of acetylenes in the presence of transition-metal catalyst Tetrahedron Letters, 25, 20, 2151-2154 Tetrahedron Letters, 25, 20, 2151-2154 Tetrahedron Letters, 25, 20, 2151-2154 1984 Refereed English Disclose to all
Seijiro Matsubara; Noriyuki Tsuboniwa; Yoshitomi Morizawa; Koichiro Oshima; hitosi Nozaki Seijiro Matsubara; Noriyuki Tsuboniwa; Yoshitomi Morizawa; Koichiro Oshima; hitosi Nozaki Seijiro Matsubara; Noriyuki Tsuboniwa; Yoshitomi Morizawa; Koichiro Oshima; hitosi Nozaki REFORMATSKY TYPE REACTION WITH NEW ALUMINIUM REAGENTS CONTAINING Al-Sn OR Al-Pb LINKAGE. REFORMATSKY TYPE REACTION WITH NEW ALUMINIUM REAGENTS CONTAINING Al-Sn OR Al-Pb LINKAGE. REFORMATSKY TYPE REACTION WITH NEW ALUMINIUM REAGENTS CONTAINING Al-Sn OR Al-Pb LINKAGE. Bulletin of the Chemical Society of Japan, 57, 11, 3242-3246 Bulletin of the Chemical Society of Japan, 57, 11, 3242-3246 Bulletin of the Chemical Society of Japan, 57, 11, 3242-3246 1984 Refereed English Disclose to all
N. Tsuboniwa; S. Matsubara; Y. Morizawa; K. Oshima; H. Nozaki N. Tsuboniwa; S. Matsubara; Y. Morizawa; K. Oshima; H. Nozaki N. Tsuboniwa; S. Matsubara; Y. Morizawa; K. Oshima; H. Nozaki Reformatsky type reaction by means of Bu<sub>3</sub>SnA1et<sub>2</sub> or Bu<sub>3</sub>Pba1et<sub>2</sub> Reformatsky type reaction by means of Bu<sub>3</sub>SnA1et<sub>2</sub> or Bu<sub>3</sub>Pba1et<sub>2</sub> Reformatsky type reaction by means of Bu<sub>3</sub>SnA1et<sub>2</sub> or Bu<sub>3</sub>Pba1et<sub>2</sub> Tetrahedron Letters, 25, 24, 2569-2572 Tetrahedron Letters, 25, 24, 2569-2572 Tetrahedron Letters, 25, 24, 2569-2572 1984 Refereed English Disclose to all
S. Kanemoto; K. Oshima; S. Matsubara; K. Takai; H. Nozaki S. Kanemoto; K. Oshima; S. Matsubara; K. Takai; H. Nozaki S. Kanemoto; K. Oshima; S. Matsubara; K. Takai; H. Nozaki Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me<sub>3</sub>SiOOSiMe<sub>3</sub> Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me<sub>3</sub>SiOOSiMe<sub>3</sub> Transition-metal catalyzed oxidation of alcohols to aldehydes and ketones by means of Me<sub>3</sub>SiOOSiMe<sub>3</sub> Tetrahedron Letters, 24, 21, 2185-2188 Tetrahedron Letters, 24, 21, 2185-2188 Tetrahedron Letters, 24, 21, 2185-2188 1983 Refereed English Disclose to all
S. Matsubara; K. Takai; H. Nozaki S. Matsubara; K. Takai; H. Nozaki S. Matsubara; K. Takai; H. Nozaki Isomerization of primary allylic alcohols to tertiary ones by means of Me<sub>3</sub>SiOOSiMe<sub>3</sub>-VO(acac)<sub>2</sub> catalyst Isomerization of primary allylic alcohols to tertiary ones by means of Me<sub>3</sub>SiOOSiMe<sub>3</sub>-VO(acac)<sub>2</sub> catalyst Isomerization of primary allylic alcohols to tertiary ones by means of Me<sub>3</sub>SiOOSiMe<sub>3</sub>-VO(acac)<sub>2</sub> catalyst Tetrahedron Letters, 24, 35, 3741-3744 Tetrahedron Letters, 24, 35, 3741-3744 Tetrahedron Letters, 24, 35, 3741-3744 1983 Refereed English Disclose to all
Seijiro Matsubara; Kazuhiko Takai; Hitosi Nozaki Seijiro Matsubara; Kazuhiko Takai; Hitosi Nozaki Seijiro Matsubara; Kazuhiko Takai; Hitosi Nozaki BAEYER-VILLIGER OXIDATION WITH Me//3SiOOSiMe//3 UNDER ASSISTANCE OF SnCl//4 OR BF//3-OEt//2. BAEYER-VILLIGER OXIDATION WITH Me//3SiOOSiMe//3 UNDER ASSISTANCE OF SnCl//4 OR BF//3-OEt//2. BAEYER-VILLIGER OXIDATION WITH Me//3SiOOSiMe//3 UNDER ASSISTANCE OF SnCl//4 OR BF//3-OEt//2. Bulletin of the Chemical Society of Japan, 56, 7, 2029-2032 Bulletin of the Chemical Society of Japan, 56, 7, 2029-2032 Bulletin of the Chemical Society of Japan, 56, 7, 2029-2032 1983 Refereed English Disclose to all
Hiroyuki Saimoto; Masaki Shinoda; Seijiro Matsubara; Koichiro Oshima; Tamejiro Hiyama; Hitosi Nozaki Hiroyuki Saimoto; Masaki Shinoda; Seijiro Matsubara; Koichiro Oshima; Tamejiro Hiyama; Hitosi Nozaki Hiroyuki Saimoto; Masaki Shinoda; Seijiro Matsubara; Koichiro Oshima; Tamejiro Hiyama; Hitosi Nozaki NEW METHODS FOR THE SYNTHESIS OF 3(2H)-FURANONES AND 2(5H)-FURANONES. NEW METHODS FOR THE SYNTHESIS OF 3(2H)-FURANONES AND 2(5H)-FURANONES. NEW METHODS FOR THE SYNTHESIS OF 3(2H)-FURANONES AND 2(5H)-FURANONES. Bulletin of the Chemical Society of Japan, 56, 10, 3088-3092 Bulletin of the Chemical Society of Japan, 56, 10, 3088-3092 Bulletin of the Chemical Society of Japan, 56, 10, 3088-3092 1983 Refereed English Disclose to all

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Title language:
Conference Activities & Talks
Title Title(Japanese) Title(English) Conference Conference(Japanese) Conference(English) Promotor Promotor(Japanese) Promotor(English) Date Language Assortment Disclose
有機金属反応剤と有機分子触媒の使い方[Invited] 有機金属反応剤と有機分子触媒の使い方 [Invited] 第34回有機合成若手セミナー「明日の有機合成を担う人のために」 第34回有機合成若手セミナー「明日の有機合成を担う人のために」 2014/08/05 Japanese Public discourse, seminar, tutorial, course, lecture and others Disclose to all
環化付加と環化反応の新しい工夫[Invited] 環化付加と環化反応の新しい工夫 [Invited] 平成24年度後期有機合成化学講習会 平成24年度後期有機合成化学講習会 2012/11/20 Japanese Public discourse, seminar, tutorial, course, lecture and others Disclose to all
Novel Synthetic Method for Heterocyclic Compounds[Invited] Novel Synthetic Method for Heterocyclic Compounds [Invited] Novel Synthetic Method for Heterocyclic Compounds [Invited] Bristol-Kyoto Organic Synthesis Workshop in Kyoto Bristol-Kyoto Organic Synthesis Workshop in Kyoto Bristol-Kyoto Organic Synthesis Workshop in Kyoto 2012/11/17 English Oral presentation(invited, special) Disclose to all
有機亜鉛反応剤系でのマイクロフローの微分的な利用[Invited] 有機亜鉛反応剤系でのマイクロフローの微分的な利用 [Invited] フロー・マイクロ合成研究会第26回公開講演会 フロー・マイクロ合成研究会第26回公開講演会 2012/08/03 Japanese Public discourse, seminar, tutorial, course, lecture and others Disclose to all
New Methods for the Preparation of Heterocyclic Compounds[Invited] New Methods for the Preparation of Heterocyclic Compounds [Invited] New Methods for the Preparation of Heterocyclic Compounds [Invited] 2nd International Collaborative and Cooperative Chemistry Symposium (ICCCS2) 2nd International Collaborative and Cooperative Chemistry Symposium (ICCCS2) 2011/11/01 English Oral presentation(invited, special) Disclose to all
Title language:
Books etc
Author Author(Japanese) Author(English) Title Title(Japanese) Title(English) Publisher Publisher(Japanese) Publisher(English) Publication date Language Type Disclose
MATSUBARA Seijiro MATSUBARA Seijiro MATSUBARA Seijiro Transition-Metal-Mediated Aromatic Ring Construction Transition-Metal-Mediated Aromatic Ring Construction Transition-Metal-Mediated Aromatic Ring Construction Wiley-VCH Wiley-VCH Wiley-VCH 2013 English Joint Work Disclose to all
MATSUBARA Seijiro 松原 誠二郎 MATSUBARA Seijiro The Chemistry of Organozinc Compounds Vol 2 The Chemistry of Organozinc Compounds Vol 2 The Chemistry of Organozinc Compounds Vol 2 Wiley-VCH Wiley-VCH Wiley-VCH 2006 Joint Work Disclose to all
MATSUBARA Seijiro MATSUBARA Seijiro MATSUBARA Seijiro Handbook of C-H Transformations Vol 2 Handbook of C-H Transformations Vol 2 Handbook of C-H Transformations Vol 2 Wiley-VCH Wiley-VCH Wiley-VCH 2005 Japanese Joint Work Disclose to all
MATSUBARA Seijiro MATSUBARA Seijiro MATSUBARA Seijiro Handbook of Functionalized Organometallics Handbook of Functionalized Organometallics Handbook of Functionalized Organometallics Wiley-VCH Wiley-VCH Wiley-VCH 2005 Joint Work Disclose to all
MATSUBARA Seijiro MATSUBARA Seijiro MATSUBARA Seijiro Modern Carbonyl Olefination Modern Carbonyl Olefination Modern Carbonyl Olefination Wiley-VCH Wiley-VCH Wiley-VCH 2004 Joint Work Disclose to all
Title language:
Awards
Title(Japanese) Title(English) Organization name(Japanese) Organization name(English) Date
井上研究奨励賞 Inoue Research Award for Young Scientists 井上科学振興財団 1986
有機合成化学協会奨励賞 Incentive Award in Synthetic Organic Chemistry, Japan 有機合成化学協会 1998
2014 ACP レクチャーシップ賞(Malaysia) 2014 ACP Lectureshipaward(Malaysia) アジア研究教育拠点事業 2013
2014 ACP レクチャーシップ賞(韓国) 2014 ACP Lectureship Award(Korea) アジア研究教育拠点事業 2013
External funds: competitive funds and Grants-in-Aid for Scientific Research (Kakenhi)
Type Position Title(Japanese) Title(English) Period
萌芽研究 Representative 有機薄膜上での有機化学反応によるナノ構造構築 2003/04/01-2005/03/31
特定領域 Representative 重水素化空間の構築と物性 2006/04/01-2008/03/31
特定領域 Representative 重水素化空間の構築 2005/04/01-2006/03/31
特定領域 Representative ポリメタル化合物による高度分子変換 2006/04/01-2007/03/31
特定領域 Representative 亜臨界水を利用する不活性炭素−水素結合の活性化 2007/04/01-2009/03/31
基盤研究(B) Representative 炭素-水素および炭素-ヘテロ原子結合活性化による新規有機合成手法の開発 2008/04/01-2011/03/31
新学術領域研究(研究領域提案型) Representative 特殊反応場の集積化 2009/07/23-2014/03/31
新学術領域研究(研究領域提案型) Assignment 反応集積化の合成化学(総括班) 2009/07/23-2015/03/31
基盤研究(B) Representative 直鎖炭化水素基を官能基として用いる分子触媒の設計 2011/04/01-2014/03/31
Teaching subject(s)
Name(Japanese) Name(English) Term Department Period
基礎有機化学A Basic Organic Chemistry A 前期 全学共通科目 2011/04-2012/03
基礎有機化学B Basic Organic Chemistry B 後期 全学共通科目 2011/04-2012/03
有機材料化学 後期 工学研究科 2011/04-2012/03
有機反応化学特論 後期 工学研究科 2011/04-2012/03
有機化学II(創成化学) 前期 工学部 2011/04-2012/03
創成化学実験Ⅰ(創成化学) 前期 工学部 2011/04-2012/03
創成化学実験Ⅱ(創成化学) 後期 工学部 2011/04-2012/03
材料有機合成化学 後期 工学部 2011/04-2012/03
科学英語(創成化学) Scientific English 前期 全学共通科目 2011/04-2012/03
有機金属化学1 前期 工学研究科 2011/04-2012/03
創成化学実験II(創成化学) Frontier Chemistry Laboratory II(Frontier Chemistry) 後期 工学部 2012/04-2013/03
創成化学実験I(創成化学) Frontier Chemistry Laboratory I(Frontier Chemistry) 前期 工学部 2012/04-2013/03
基礎有機化学A Basic Organic Chemistry A 前期 全学共通科目 2012/04-2013/03
基礎有機化学B Basic Organic Chemistry B 後期 全学共通科目 2012/04-2013/03
有機化学II(創成化学) Organic Chemistry II (Frontier Chemistry) 前期 工学部 2012/04-2013/03
有機反応化学特論 Organic Reaction Chemistry, Advanced 後期 工学研究科 2012/04-2013/03
有機材料化学 Chemistry of Organic Materials 後期 工学研究科 2012/04-2013/03
有機材料合成化学 Synthesis of Organic Materials 後期 工学研究科 2012/04-2013/03
有機金属化学1 Organotransition Metal Chemistry 1 前期 工学研究科 2012/04-2013/03
材料化学特別実験及演習 Laboratory and Exercise in Material Chemistry 通年 工学研究科 2012/04-2013/03
材料化学特論第二 Material Chemistry Adv. II 後期 工学研究科 2012/04-2013/03
材料有機合成化学 Organic Material Synthetic Chemistry 後期 工学部 2012/04-2013/03
研究論文 Master's Thesis 通年 工学研究科 2012/04-2013/03
モノつくりの科学と技術 Science and Technology for Making Substances 前期 工学研究科 2012/04-2013/03
科学英語(創成化学) Scientific English 前期 全学共通科目 2012/04-2013/03
有機化学II(創成化学) Organic Chemistry II (Frontier Chemistry) 前期 工学部 2013/04-2014/03
化学のフロンティア(創成化学) Frontier Chemistry (Frontier Chemistry) 前期 工学部 2013/04-2014/03
創成化学実験I(創成化学) Frontier Chemistry Laboratory I(Frontier Chemistry) 前期 工学部 2013/04-2014/03
創成化学実験II(創成化学) Frontier Chemistry Laboratory II(Frontier Chemistry) 後期 工学部 2013/04-2014/03
材料有機合成化学 Organic Material Synthetic Chemistry 後期 工学部 2013/04-2014/03
有機材料化学 Chemistry of Organic Materials 後期 工学研究科 2013/04-2014/03
有機金属化学1 Organotransition Metal Chemistry 1 前期 工学研究科 2013/04-2014/03
有機反応化学特論 Organic Reaction Chemistry, Advanced 後期 工学研究科 2013/04-2014/03
基礎有機化学A Basic Organic Chemistry A 前期 全学共通科目 2013/04-2014/03
基礎有機化学B Basic Organic Chemistry B 後期 全学共通科目 2013/04-2014/03
科学英語(創成化学) Scientific English 前期 全学共通科目 2013/04-2014/03
有機化学II(創成化学) Organic Chemistry II (Frontier Chemistry) 前期 工学部 2014/04-2015/03
創成化学実験I(創成化学) Frontier Chemistry Laboratory I(Frontier Chemistry) 前期 工学部 2014/04-2015/03
創成化学実験II(創成化学) Frontier Chemistry Laboratory II(Frontier Chemistry) 後期 工学部 2014/04-2015/03
材料有機合成化学 Organic Material Synthetic Chemistry 後期 工学部 2014/04-2015/03
有機材料化学 Chemistry of Organic Materials 後期 工学研究科 2014/04-2015/03
有機材料合成化学 Synthesis of Organic Materials 後期 工学研究科 2014/04-2015/03
有機金属化学1 Organotransition Metal Chemistry 1 前期 工学研究科 2014/04-2015/03
有機反応化学特論 Organic Reaction Chemistry, Advanced 後期 工学研究科 2014/04-2015/03
基礎有機化学B Basic Organic Chemistry B 後期 全学共通科目 2014/04-2015/03
科学英語(創成化学) Scientific English 前期 全学共通科目 2014/04-2015/03
創成化学実験II(創成化学) Frontier Chemistry Laboratory II(Frontier Chemistry) 後期 工学部 2015/04-2016/03
創成化学実験I(創成化学) Frontier Chemistry Laboratory I(Frontier Chemistry) 前期 工学部 2015/04-2016/03
基礎有機化学II Basic Organic Chemistry II 後期 全学共通科目 2015/04-2016/03
有機化学II(創成化学) Organic Chemistry II (Frontier Chemistry) 前期 工学部 2015/04-2016/03
有機反応化学特論 Organic Reaction Chemistry, Advanced 後期 工学研究科 2015/04-2016/03
有機材料化学 Chemistry of Organic Materials 後期 工学研究科 2015/04-2016/03
材料有機合成化学 Organic Material Synthetic Chemistry 後期 工学部 2015/04-2016/03
科学英語(創生化学) Scientific English 前期 工学部 2015/04-2016/03

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School management (title, position)
Title Period
桂キャンパス整備専門委員会 委員 2010/04/01-2010/09/30
全学共通教育システム委員会 委員 2010/04/01-2011/03/31
外国語教育専門委員会 委員長 2010/04/01-2011/03/31
人権委員会 委員 2013/04/01-2015/03/31
Other activities (primary and secondary education)
Title Activity School Prefecture Date
子どもの知的好奇心をくすぐる体験授業 「有機化学−結合について−」講義及び実習 京都府立亀岡高校 京都府 2014/02/05
滋賀県立膳所高校SSH 大学研究室実習「分子の分析,構造決定」 滋賀県立膳所高校 滋賀県 2014/09/