下川 淳

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Name(Kanji/Kana/Abecedarium Latinum)
下川 淳/シモカワ ジュン/Shimokawa, Jun
Primary Affiliation(Org1/Job title)
Graduate Schools Science/Associate Professor
E-mail Address
E-mail address
shimokawa @ kuchem.kyoto-u.ac.jp
Academic Degree
Field(Japanese) Field(English) University(Japanese) University(English) Method
修士(薬学) 東京大学
博士(薬学) 東京大学
Language of Instruction
Language
English
Personal Website(s) (URL(s))
URL
http://kuchem.kyoto-u.ac.jp/orgchem/yorimitsu_lab/j_shimokawa.html
ORCID ID
https://orcid.org/0000-0002-4023-4640
researchmap URL
https://researchmap.jp/jun_shimokawa
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
Atsushi Kaga, Tomohiro Fukushima, Jun Shimokawa, Masato Kitamura Atsushi Kaga, Tomohiro Fukushima, Jun Shimokawa, Masato Kitamura Atsushi Kaga, Tomohiro Fukushima, Jun Shimokawa, Masato Kitamura Photoredox Fischer Indole Synthesis Photoredox Fischer Indole Synthesis Photoredox Fischer Indole Synthesis Synthesis Synthesis Synthesis 2019/05 Refereed Disclose to all
Jun Shimokawa, Kazuo Nagasawa Jun Shimokawa, Kazuo Nagasawa Jun Shimokawa, Kazuo Nagasawa Identification of Target Protein for Batzelladines as CD4 Identification of Target Protein for Batzelladines as CD4 Identification of Target Protein for Batzelladines as CD4 Heterocycles, 99, 1, 521-533 Heterocycles, 99, 1, 521-533 Heterocycles, 99, 1, 521-533 2018/12 Refereed English Disclose to all
Hiroki Yamagishi, Shun Tsuchiya, Hayate Saito, Keisuke Nogi, Jun Shimokawa, Hideki Yorimitsu Hiroki Yamagishi, Shun Tsuchiya, Hayate Saito, Keisuke Nogi, Jun Shimokawa, Hideki Yorimitsu Hiroki Yamagishi, Shun Tsuchiya, Hayate Saito, Keisuke Nogi, Jun Shimokawa, Hideki Yorimitsu Four-component Coupling Strategy for 2,3,4-Trisubstituted 3,4-Dihydroquinoline Four-component Coupling Strategy for 2,3,4-Trisubstituted 3,4-Dihydroquinoline Four-component Coupling Strategy for 2,3,4-Trisubstituted 3,4-Dihydroquinoline Heterocycles, 99, 1, 301-309 Heterocycles, 99, 1, 301-309 Heterocycles, 99, 1, 301-309 2018/10 Refereed English Disclose to all
Kazuya Douki, Jun Shimokawa, Masato Kitamura Kazuya Douki, Jun Shimokawa, Masato Kitamura Kazuya Douki, Jun Shimokawa, Masato Kitamura Synthesis of the core structure of phalarine Synthesis of the core structure of phalarine Synthesis of the core structure of phalarine Organic & Biomolecular Chemistry Organic & Biomolecular Chemistry Organic & Biomolecular Chemistry 2018/10 Refereed Disclose to all
Shimokawa Jun Shimokawa Jun Shimokawa Jun Natural Product Synthesis as a Source of Inspiration and Discovery Natural Product Synthesis as a Source of Inspiration and Discovery Natural Product Synthesis as a Source of Inspiration and Discovery JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 76, 5, 458-461 JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 76, 5, 458-461 JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 76, 5, 458-461 2018/05 Refereed Disclose to all
Shimokawa Jun Shimokawa Jun Shimokawa Jun Synthetic Studies on Heteropolycyclic Natural Products: Development of Divergent Strategy Synthetic Studies on Heteropolycyclic Natural Products: Development of Divergent Strategy Synthetic Studies on Heteropolycyclic Natural Products: Development of Divergent Strategy CHEMICAL & PHARMACEUTICAL BULLETIN, 66, 2, 105-115 CHEMICAL & PHARMACEUTICAL BULLETIN, 66, 2, 105-115 CHEMICAL & PHARMACEUTICAL BULLETIN, 66, 2, 105-115 2018/02 Refereed Disclose to all
Shimokawa Jun, Fukuyama Tohru Shimokawa Jun, Fukuyama Tohru Shimokawa Jun, Fukuyama Tohru Synthetic Studies on Heteropolycyclic Natural Products: Strategies via Novel Reactions and Reactivities Synthetic Studies on Heteropolycyclic Natural Products: Strategies via Novel Reactions and Reactivities Synthetic Studies on Heteropolycyclic Natural Products: Strategies via Novel Reactions and Reactivities JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 75, 11, 1115-1124 JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 75, 11, 1115-1124 JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 75, 11, 1115-1124 2017/11 Refereed Disclose to all
Abe Kazuhiro, Shimokawa Jun, Naito Mao, Munson Keith, Vagin Olga, Sachs George, Suzuki Hiroshi, Tani Kazutoshi, Fujiyoshi Yoshinori Abe Kazuhiro, Shimokawa Jun, Naito Mao, Munson Keith, Vagin Olga, Sachs George, Suzuki Hiroshi, Tani Kazutoshi, Fujiyoshi Yoshinori Abe Kazuhiro, Shimokawa Jun, Naito Mao, Munson Keith, Vagin Olga, Sachs George, Suzuki Hiroshi, Tani Kazutoshi, Fujiyoshi Yoshinori The cryo-EM structure of gastric H+, K+-ATPase with bound BYK99, a high-affinity member of K+-competitive, imidazo[1,2-a]pyridine inhibitors The cryo-EM structure of gastric H+, K+-ATPase with bound BYK99, a high-affinity member of K+-competitive, imidazo[1,2-a]pyridine inhibitors The cryo-EM structure of gastric H+, K+-ATPase with bound BYK99, a high-affinity member of K+-competitive, imidazo[1,2-a]pyridine inhibitors SCIENTIFIC REPORTS, 7 SCIENTIFIC REPORTS, 7 SCIENTIFIC REPORTS, 7 2017/07/26 Refereed Disclose to all
Kazuya Douki, Hiroyuki Ono, Tohru Taniguchi, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama Kazuya Douki, Hiroyuki Ono, Tohru Taniguchi, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama Kazuya Douki, Hiroyuki Ono, Tohru Taniguchi, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama Enantioselective Total Synthesis of (+)-Hinckdentine A via a Catalytic Dearomatization Approach Enantioselective Total Synthesis of (+)-Hinckdentine A via a Catalytic Dearomatization Approach Enantioselective Total Synthesis of (+)-Hinckdentine A via a Catalytic Dearomatization Approach Journal of the American Chemical Society, 138, 44, 14578-14581 Journal of the American Chemical Society, 138, 44, 14578-14581 Journal of the American Chemical Society, 138, 44, 14578-14581 2016/10 Refereed Disclose to all
Takaaki Harada, Jun Shimokawa, Tohru Fukuyama Takaaki Harada, Jun Shimokawa, Tohru Fukuyama Takaaki Harada, Jun Shimokawa, Tohru Fukuyama Unified Total Synthesis of Five Gelsedine-Type Alkaloids: (−)-Gelsenicine, (−)-Gelsedine, (−)-Gelsedilam, (−)-14- Hydroxygelsenicine, and (−)-14,15-Dihydroxygelsenicine Unified Total Synthesis of Five Gelsedine-Type Alkaloids: (−)-Gelsenicine, (−)-Gelsedine, (−)-Gelsedilam, (−)-14- Hydroxygelsenicine, and (−)-14,15-Dihydroxygelsenicine Unified Total Synthesis of Five Gelsedine-Type Alkaloids: (−)-Gelsenicine, (−)-Gelsedine, (−)-Gelsedilam, (−)-14- Hydroxygelsenicine, and (−)-14,15-Dihydroxygelsenicine Organic Letters, 18, 18, 4622-4625 Organic Letters, 18, 18, 4622-4625 Organic Letters, 18, 18, 4622-4625 2016/08 Refereed Disclose to all
Hirotatsu Unihara, Tomomi Yoshino, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama Hirotatsu Unihara, Tomomi Yoshino, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama Hirotatsu Unihara, Tomomi Yoshino, Jun Shimokawa, Masato Kitamura, Tohru Fukuyama Development of a Divergent Synthetic Route to the Erythrina Alkaloids: Asymmetric Syntheses of 8-Oxo-erythrinine, Crystamidine, 8-Oxo-erythraline, and Erythraline Development of a Divergent Synthetic Route to the Erythrina Alkaloids: Asymmetric Syntheses of 8-Oxo-erythrinine, Crystamidine, 8-Oxo-erythraline, and Erythraline Development of a Divergent Synthetic Route to the Erythrina Alkaloids: Asymmetric Syntheses of 8-Oxo-erythrinine, Crystamidine, 8-Oxo-erythraline, and Erythraline Angewandte Chemie, International Edition, 55, 24, 6915-6918 Angewandte Chemie, International Edition, 55, 24, 6915-6918 Angewandte Chemie, International Edition, 55, 24, 6915-6918 2016/05 Refereed English Research paper(scientific journal) Disclose to all
Jun Shimokawa, Koji Chiyoda, Hirotatsu Umihara, Tohru Fukuyama Jun Shimokawa, Koji Chiyoda, Hirotatsu Umihara, Tohru Fukuyama Jun Shimokawa, Koji Chiyoda, Hirotatsu Umihara, Tohru Fukuyama Antiproliferative Activity of Amathaspiramide Alkaloids and Analogs Antiproliferative Activity of Amathaspiramide Alkaloids and Analogs Antiproliferative Activity of Amathaspiramide Alkaloids and Analogs Chemical and Pharmaceutical Bulletin, 64, 8, 1239-1241 Chemical and Pharmaceutical Bulletin, 64, 8, 1239-1241 Chemical and Pharmaceutical Bulletin, 64, 8, 1239-1241 2016/05 Refereed English Research paper(scientific journal) Disclose to all
Ideue E, Shimokawa J, Fukuyama T Ideue E, Shimokawa J, Fukuyama T Ideue E, Shimokawa J, Fukuyama T Synthesis of the Common Core Structure of the Stemofoline Alkaloids. Synthesis of the Common Core Structure of the Stemofoline Alkaloids. Synthesis of the Common Core Structure of the Stemofoline Alkaloids. Organic Letters, 17, 20, 4964-4967 Organic Letters, 17, 20, 4964-4967 Organic Letters, 17, 20, 4964-4967 2015/10 Refereed Disclose to all
Jun Shimokawa Jun Shimokawa Jun Shimokawa Divergent strategy in natural product total synthesis Divergent strategy in natural product total synthesis Divergent strategy in natural product total synthesis Tetrahedron Letters, 55, 6156-6162 Tetrahedron Letters, 55, 6156-6162 Tetrahedron Letters, 55, 6156-6162 2014/11 Refereed English Research paper(scientific journal) Disclose to all
Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa, Tohru Fukuyama Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa, Tohru Fukuyama Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa, Tohru Fukuyama Erratum: Total synthesis of tryprostatins A and B (Angewandte Chemie - International Edition (2010) (49)) Erratum: Total synthesis of tryprostatins A and B (Angewandte Chemie - International Edition (2010) (49)) Erratum: Total synthesis of tryprostatins A and B (Angewandte Chemie - International Edition (2010) (49)) Angewandte Chemie International Edition, 53, 8808 Angewandte Chemie International Edition, 53, 8808 Angewandte Chemie International Edition, 53, 8808 2014/08 Refereed Disclose to all
Ren Takeuchi, Jun Shimokawa, Tohru Fukuyama Ren Takeuchi, Jun Shimokawa, Tohru Fukuyama Ren Takeuchi, Jun Shimokawa, Tohru Fukuyama Development of a route to chiral epidithiodioxopiperazine moieties and application to the asymmetric synthesis of (+)-hyalodendrin Development of a route to chiral epidithiodioxopiperazine moieties and application to the asymmetric synthesis of (+)-hyalodendrin Development of a route to chiral epidithiodioxopiperazine moieties and application to the asymmetric synthesis of (+)-hyalodendrin Chemical Science, 5, 2003-2006 Chemical Science, 5, 2003-2006 Chemical Science, 5, 2003-2006 2014/05 Refereed Disclose to all
Kaise H, Shimokawa J, Fukuyama T Kaise H, Shimokawa J, Fukuyama T Kaise H, Shimokawa J, Fukuyama T TMSCN/DBU-mediated facile redox transformation of α,β-unsaturated aldehydes to carboxylic acid derivatives. TMSCN/DBU-mediated facile redox transformation of α,β-unsaturated aldehydes to carboxylic acid derivatives. TMSCN/DBU-mediated facile redox transformation of α,β-unsaturated aldehydes to carboxylic acid derivatives. Organic letters, 16, 3, 727-729 Organic letters, 16, 3, 727-729 Organic letters, 16, 3, 727-729 2014/02 Refereed Disclose to all
Katsushi Kitahara, Jun Shimokawa, Tohru Fukuyama Katsushi Kitahara, Jun Shimokawa, Tohru Fukuyama Katsushi Kitahara, Jun Shimokawa, Tohru Fukuyama Stereoselective synthesis of spirotryprostatin A Stereoselective synthesis of spirotryprostatin A Stereoselective synthesis of spirotryprostatin A Chemical Science, 5, 904-907 Chemical Science, 5, 904-907 Chemical Science, 5, 904-907 2014/01 Refereed Disclose to all
Yuri Iwai, Takashi Ozaki, Ryo Takita, Masanobu Uchiyama, Jun Shimokawa, Tohru Fukuyama Yuri Iwai, Takashi Ozaki, Ryo Takita, Masanobu Uchiyama, Jun Shimokawa, Tohru Fukuyama Yuri Iwai, Takashi Ozaki, Ryo Takita, Masanobu Uchiyama, Jun Shimokawa, Tohru Fukuyama Modified McFadyen-Stevens reaction for a versatile synthesis of aliphatic/aromatic aldehydes: Design, optimization, and mechanistic investigations Modified McFadyen-Stevens reaction for a versatile synthesis of aliphatic/aromatic aldehydes: Design, optimization, and mechanistic investigations Modified McFadyen-Stevens reaction for a versatile synthesis of aliphatic/aromatic aldehydes: Design, optimization, and mechanistic investigations Chemical Science, 4, 1111-1119 Chemical Science, 4, 1111-1119 Chemical Science, 4, 1111-1119 2013/03 Refereed Disclose to all
Eiji Ideue, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Eiji Ideue, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Convenient Synthesis of alpha-Diazoacetates from alpha-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate Convenient Synthesis of alpha-Diazoacetates from alpha-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate Org. Synth., 89, 501-509 Org. Synth., 89, 501-509 , 89, 501-509 2012/05/25 Refereed Disclose to all
Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Efficient Synthesis of Oxime Using O-TBS-N-Tosylhydroxylamine: Preparation of (2Z)-4-(Benzyloxy)but-2-enal Oxime Efficient Synthesis of Oxime Using O-TBS-N-Tosylhydroxylamine: Preparation of (2Z)-4-(Benzyloxy)but-2-enal Oxime Org. Synth., 89, 480-490 Org. Synth., 89, 480-490 , 89, 480-490 2012/05/16 Refereed Disclose to all
Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Total Synthesis of Gelsemoxonine Total Synthesis of Gelsemoxonine Pure Appl. Chem., 84, 7, 1643-1650 Pure Appl. Chem., 84, 7, 1643-1650 , 84, 7, 1643-1650 2012/05/02 Refereed Disclose to all
Koji Chiyoda, Jun Shimokawa, and Tohru Fukuyama Koji Chiyoda, Jun Shimokawa, and Tohru Fukuyama Koji Chiyoda, Jun Shimokawa, and Tohru Fukuyama Total Syntheses of All the Amathaspiramides Total Syntheses of All the Amathaspiramides Total Syntheses of All the Amathaspiramides Angewandte Chemie International Edition, 51, 10, 2505-2508 Angewandte Chemie International Edition, 51, 10, 2505-2508 Angewandte Chemie International Edition, 51, 10, 2505-2508 2012/01/27 Refereed Disclose to all
Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Total Synthesis of Gelsemoxonine Total Synthesis of Gelsemoxonine J. Am. Chem. Soc., 133, 44, 17634-17637 J. Am. Chem. Soc., 133, 44, 17634-17637 , 133, 44, 17634-17637 2011/10/08 Refereed Disclose to all
Yuji Fujita, Mitsuhiro Yonehara, Katsushi Kitahara, Jun Shimokawa, Yuichi Hashimoto, and Minoru Ishikawa Yuji Fujita, Mitsuhiro Yonehara, Katsushi Kitahara, Jun Shimokawa, Yuichi Hashimoto, and Minoru Ishikawa Confirmation of Molecular Planarity Disruption Effect on Aqueous Solubility Improvement of β-Naphthoflavone Analogs Confirmation of Molecular Planarity Disruption Effect on Aqueous Solubility Improvement of β-Naphthoflavone Analogs HETEROCYCLES, 83, 11, 2563-2575 HETEROCYCLES, 83, 11, 2563-2575 , 83, 11, 2563-2575 2011/10/05 Refereed Disclose to all
Takayuki Yamakawa, Eiji Ideue, Yuzo Iwaki, Ayumu Sato, Hidetoshi Tokuyama, Jun Shimokawa, Tohru Fukuyama Takayuki Yamakawa, Eiji Ideue, Yuzo Iwaki, Ayumu Sato, Hidetoshi Tokuyama, Jun Shimokawa, Tohru Fukuyama Total synthesis of tryprostatins A and B Total synthesis of tryprostatins A and B Tetrahedron, 67, 35, 6547 Tetrahedron, 67, 35, 6547 , 67, 35, 6547 2011/06/02 Refereed Disclose to all
Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa and Tohru Fukuyama Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa and Tohru Fukuyama Total Synthesis of Tryprostatins A and B Total Synthesis of Tryprostatins A and B Angew. Chem. Int. Ed., 49, 48, 9262-9265 Angew. Chem. Int. Ed., 49, 48, 9262-9265 , 49, 48, 9262-9265 2010/10/28 Refereed Disclose to all
Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama O-TBS-N-tosylhydroxylamine: A Reagent for Facile Conversion of Alcohols to Oximes O-TBS-N-tosylhydroxylamine: A Reagent for Facile Conversion of Alcohols to Oximes Org. Lett., 10, 11, 2259-2261 Org. Lett., 10, 11, 2259-2261 , 10, 11, 2259-2261 2008/04/30 Refereed Disclose to all
Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama N,N'-Ditosylhydrazine: A Convenient Reagent for Facile Synthesis of Diazoacetates N,N'-Ditosylhydrazine: A Convenient Reagent for Facile Synthesis of Diazoacetates Org. Lett., 9, 16, 3195-3197 Org. Lett., 9, 16, 3195-3197 , 9, 16, 3195-3197 2007/07/13 Refereed Disclose to all
Kazuo Nagasawa, Jun Shimokawa Kazuo Nagasawa, Jun Shimokawa Synthetic studies on cyclic guanidine natural products for the elucidation of their controlling mechanism of protein-protein interaction Synthetic studies on cyclic guanidine natural products for the elucidation of their controlling mechanism of protein-protein interaction J. Synth. Org. Chem., Jpn., 64, 5, 539-547 J. Synth. Org. Chem., Jpn., 64, 5, 539-547 , 64, 5, 539-547 2007/05/01 Refereed Disclose to all
Jun Shimokawa, Yumi Iijima, Yuichi Hashimoto, Harumi Chiba, Haruo Tanaka, and Kazuo Nagasawa Jun Shimokawa, Yumi Iijima, Yuichi Hashimoto, Harumi Chiba, Haruo Tanaka, and Kazuo Nagasawa Synthesis and Biological Activities on Batzelladine Derivatives Synthesis and Biological Activities on Batzelladine Derivatives HETEROCYCLES, 72, 145-150 HETEROCYCLES, 72, 145-150 , 72, 145-150 2007/01/12 Refereed Disclose to all
Jun Shimokawa, Takanori Ishiwata, Koji Shirai, Hiroyuki Koshino, Aya Tanatani, Tadashi Nakata, Yuichi Hashimoto, Kazuo Nagasawa Jun Shimokawa, Takanori Ishiwata, Koji Shirai, Hiroyuki Koshino, Aya Tanatani, Tadashi Nakata, Yuichi Hashimoto, Kazuo Nagasawa Total Synthesis of (+)-Batzelladine A and (-)-Batzelladine D, and Identification of Their Target Protein Total Synthesis of (+)-Batzelladine A and (-)-Batzelladine D, and Identification of Their Target Protein Chem. Eur. J., 11, 23, 6878-6888 Chem. Eur. J., 11, 23, 6878-6888 , 11, 23, 6878-6888 2005/09/14 Refereed Disclose to all
Jun Shimokawa, Koji Shirai, Aya Tanatani, Yuichi Hashimoto, Kazuo Nagasawa Jun Shimokawa, Koji Shirai, Aya Tanatani, Yuichi Hashimoto, Kazuo Nagasawa Enantioselective Total Synthesis of Batzelladine A Enantioselective Total Synthesis of Batzelladine A Angew. Chem. Int. Ed., 43, 12, 1559-1562 Angew. Chem. Int. Ed., 43, 12, 1559-1562 , 43, 12, 1559-1562 2004/03/09 Refereed Disclose to all
Eiji Ideue, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Eiji Ideue, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Convenient Synthesis of alpha-Diazoacetates from alpha-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate Convenient Synthesis of alpha-Diazoacetates from alpha-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate Org. Synth., 89, 501-509 , 89, 501-509 Org. Synth., 89, 501-509 2012/05/25 Refereed Disclose to all
Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa and Tohru Fukuyama Efficient Synthesis of Oxime Using O-TBS-N-Tosylhydroxylamine: Preparation of (2Z)-4-(Benzyloxy)but-2-enal Oxime Efficient Synthesis of Oxime Using O-TBS-N-Tosylhydroxylamine: Preparation of (2Z)-4-(Benzyloxy)but-2-enal Oxime Org. Synth., 89, 480-490 , 89, 480-490 Org. Synth., 89, 480-490 2012/05/16 Refereed Disclose to all
Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Total Synthesis of Gelsemoxonine Total Synthesis of Gelsemoxonine Pure Appl. Chem., 84, 7, 1643-1650 , 84, 7, 1643-1650 Pure Appl. Chem., 84, 7, 1643-1650 2012/05/02 Refereed Disclose to all
Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Jun Shimokawa, Takaaki Harada, Satoshi Yokoshima, and Tohru Fukuyama Total Synthesis of Gelsemoxonine Total Synthesis of Gelsemoxonine J. Am. Chem. Soc., 133, 44, 17634-17637 , 133, 44, 17634-17637 J. Am. Chem. Soc., 133, 44, 17634-17637 2011/10/08 Refereed Disclose to all
Yuji Fujita, Mitsuhiro Yonehara, Katsushi Kitahara, Jun Shimokawa, Yuichi Hashimoto, and Minoru Ishikawa Yuji Fujita, Mitsuhiro Yonehara, Katsushi Kitahara, Jun Shimokawa, Yuichi Hashimoto, and Minoru Ishikawa Confirmation of Molecular Planarity Disruption Effect on Aqueous Solubility Improvement of β-Naphthoflavone Analogs Confirmation of Molecular Planarity Disruption Effect on Aqueous Solubility Improvement of β-Naphthoflavone Analogs HETEROCYCLES, 83, 11, 2563-2575 , 83, 11, 2563-2575 HETEROCYCLES, 83, 11, 2563-2575 2011/10/05 Refereed Disclose to all
Takayuki Yamakawa, Eiji Ideue, Yuzo Iwaki, Ayumu Sato, Hidetoshi Tokuyama, Jun Shimokawa, Tohru Fukuyama Takayuki Yamakawa, Eiji Ideue, Yuzo Iwaki, Ayumu Sato, Hidetoshi Tokuyama, Jun Shimokawa, Tohru Fukuyama Total synthesis of tryprostatins A and B Total synthesis of tryprostatins A and B Tetrahedron, 67, 35, 6547 , 67, 35, 6547 Tetrahedron, 67, 35, 6547 2011/06/02 Refereed Disclose to all
Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa and Tohru Fukuyama Takayuki Yamakawa, Eiji Ideue, Jun Shimokawa and Tohru Fukuyama Total Synthesis of Tryprostatins A and B Total Synthesis of Tryprostatins A and B Angew. Chem. Int. Ed., 49, 48, 9262-9265 , 49, 48, 9262-9265 Angew. Chem. Int. Ed., 49, 48, 9262-9265 2010/10/28 Refereed Disclose to all
Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama Katsushi Kitahara, Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama O-TBS-N-tosylhydroxylamine: A Reagent for Facile Conversion of Alcohols to Oximes O-TBS-N-tosylhydroxylamine: A Reagent for Facile Conversion of Alcohols to Oximes Org. Lett., 10, 11, 2259-2261 , 10, 11, 2259-2261 Org. Lett., 10, 11, 2259-2261 2008/04/30 Refereed Disclose to all
Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama Tatsuya Toma, Jun Shimokawa, and Tohru Fukuyama N,N'-Ditosylhydrazine: A Convenient Reagent for Facile Synthesis of Diazoacetates N,N'-Ditosylhydrazine: A Convenient Reagent for Facile Synthesis of Diazoacetates Org. Lett., 9, 16, 3195-3197 , 9, 16, 3195-3197 Org. Lett., 9, 16, 3195-3197 2007/07/13 Refereed Disclose to all
Kazuo Nagasawa, Jun Shimokawa Kazuo Nagasawa, Jun Shimokawa Synthetic studies on cyclic guanidine natural products for the elucidation of their controlling mechanism of protein-protein interaction Synthetic studies on cyclic guanidine natural products for the elucidation of their controlling mechanism of protein-protein interaction J. Synth. Org. Chem., Jpn., 64, 5, 539-547 , 64, 5, 539-547 J. Synth. Org. Chem., Jpn., 64, 5, 539-547 2007/05/01 Refereed Disclose to all
Jun Shimokawa, Yumi Iijima, Yuichi Hashimoto, Harumi Chiba, Haruo Tanaka, and Kazuo Nagasawa Jun Shimokawa, Yumi Iijima, Yuichi Hashimoto, Harumi Chiba, Haruo Tanaka, and Kazuo Nagasawa Synthesis and Biological Activities on Batzelladine Derivatives Synthesis and Biological Activities on Batzelladine Derivatives HETEROCYCLES, 72, 145-150 , 72, 145-150 HETEROCYCLES, 72, 145-150 2007/01/12 Refereed Disclose to all
Jun Shimokawa, Takanori Ishiwata, Koji Shirai, Hiroyuki Koshino, Aya Tanatani, Tadashi Nakata, Yuichi Hashimoto, Kazuo Nagasawa Jun Shimokawa, Takanori Ishiwata, Koji Shirai, Hiroyuki Koshino, Aya Tanatani, Tadashi Nakata, Yuichi Hashimoto, Kazuo Nagasawa Total Synthesis of (+)-Batzelladine A and (-)-Batzelladine D, and Identification of Their Target Protein Total Synthesis of (+)-Batzelladine A and (-)-Batzelladine D, and Identification of Their Target Protein Chem. Eur. J., 11, 23, 6878-6888 , 11, 23, 6878-6888 Chem. Eur. J., 11, 23, 6878-6888 2005/09/14 Refereed Disclose to all
Jun Shimokawa, Koji Shirai, Aya Tanatani, Yuichi Hashimoto, Kazuo Nagasawa Jun Shimokawa, Koji Shirai, Aya Tanatani, Yuichi Hashimoto, Kazuo Nagasawa Enantioselective Total Synthesis of Batzelladine A Enantioselective Total Synthesis of Batzelladine A Angew. Chem. Int. Ed., 43, 12, 1559-1562 , 43, 12, 1559-1562 Angew. Chem. Int. Ed., 43, 12, 1559-1562 2004/03/09 Refereed Disclose to all

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Title language:
Awards
Title(Japanese) Title(English) Organization name(Japanese) Organization name(English) Date
平成30年度 科学技術分野の文部科学大臣表彰 若手科学者賞 The Young Scientists’ Prize, The Commendation for Science and Technology 文部科学省 Minister of Education, Culture, Sports, Science and Technology 2018/04/17
Chemist Award BCA 2017 Chemist Award BCA 2017 公益財団法人MSD生命科学財団 MSD Life Science Foundation 2017/12/09
平成29年度 日本薬学会奨励賞 The Pharmaceutical Society of Japan Award for Young Scientists 日本薬学会 The Pharmaceutical Society of Japan 2017/03/24
Asian Core Program / Advanced Research Network Lectureship Award (China) Asian Core Program / Advanced Research Network Lectureship Award (China) Advanced Research Network for Asian Cutting-Edge Organic Chemistry Advanced Research Network for Asian Cutting-Edge Organic Chemistry 2016/10/30
Asian Core Program / Advanced Research Network Lectureship Award (Malaysia) Asian Core Program / Advanced Research Network Lectureship Award (China) Advanced Research Network for Asian Cutting-Edge Organic Chemistry Advanced Research Network for Asian Cutting-Edge Organic Chemistry 2016/10/30
有機合成化学協会研究企画賞(田辺三菱製薬) Mitsubishi Tanabe Pharma Corporation Award in Synthetic Organic Chemistry, Japan 有機合成化学協会 The Society of Synthetic Organic Chemistry, Japan 2015/02/19
Thieme Chemistry Journals Award 2014 Thieme Chemistry Journals Award 2014 Georg Thieme Verlag Stuttgardt, New York Georg Thieme Verlag Stuttgardt, New York 2014/12/02
天然物化学談話会奨励賞 Young Scientist’s Research Award in Natural Product Chemistry 天然物化学談話会 2012/07/07
External funds: competitive funds and Grants-in-Aid for Scientific Research (Kakenhi)
Type Position Title(Japanese) Title(English) Period
若手研究(A) Representative 中枢神経疾患の理解と治療を目指したエリスリナアルカロイド類縁体の網羅的合成研究 (平成29年度分) 2017/04/01-2018/03/31
若手研究(A) Representative 中枢神経疾患の理解と治療を目指したエリスリナアルカロイド類縁体の網羅的合成研究 (平成29年度分) 2017/04/01-2018/03/31
若手研究(A) Representative 中枢神経疾患の理解と治療を目指したエリスリナアルカロイド類縁体の網羅的合成研究 (平成30年度分) 2018/04/01-2019/03/31
Teaching subject(s)
Name(Japanese) Name(English) Term Department Period
化学課題研究14 Special study course II (Chemistry) 14 通年 理学部 2018/04-2019/03
基礎有機化学I Basic Organic Chemistry I 前期 全学共通科目 2018/04-2019/03
有機化学ゼミナールIIA Seminar on Organic Chemistry IIA 前期 理学研究科 2018/04-2019/03
有機化学ゼミナールIIB Seminar on Organic Chemistry IIB 後期 理学研究科 2018/04-2019/03
有機化学ゼミナールIIC Seminar on Organic Chemistry IIC 前期 理学研究科 2018/04-2019/03
有機化学ゼミナールIID Seminar on Organic Chemistry IID 後期 理学研究科 2018/04-2019/03
有機化学演習IIA Advanced Organic Chemistry IIA 前期 理学研究科 2018/04-2019/03
有機化学演習IIB Advanced Organic Chemistry IIB 後期 理学研究科 2018/04-2019/03
有機化学演習IIC Advanced Organic Chemistry IIC 前期 理学研究科 2018/04-2019/03
有機化学演習IID Advanced Organic Chemistry IID 後期 理学研究科 2018/04-2019/03
有機金属化学論 Organometallic Chemistry 後期 理学研究科 2018/04-2019/03
現代有機化学論 Topics in Current Organic Chemistry 後期 理学研究科 2018/04-2019/03
化学課題研究14 Special study course II (Chemistry) 14 通年 理学部 2019/04-2020/03
基礎化学実験 Fundamental Chemical Experiments 前期 全学共通科目 2019/04-2020/03
基礎有機化学I Basic Organic Chemistry I 前期 全学共通科目 2019/04-2020/03
有機化学ゼミナールIIA Seminar on Organic Chemistry IIA 前期 理学研究科 2019/04-2020/03
有機化学ゼミナールIIB Seminar on Organic Chemistry IIB 後期 理学研究科 2019/04-2020/03
有機化学ゼミナールIIC Seminar on Organic Chemistry IIC 前期 理学研究科 2019/04-2020/03
有機化学ゼミナールIID Seminar on Organic Chemistry IID 後期 理学研究科 2019/04-2020/03
有機化学演習IIA Advanced Organic Chemistry IIA 前期 理学研究科 2019/04-2020/03
有機化学演習IIB Advanced Organic Chemistry IIB 後期 理学研究科 2019/04-2020/03
有機化学演習IIC Advanced Organic Chemistry IIC 前期 理学研究科 2019/04-2020/03
有機化学演習IID Advanced Organic Chemistry IID 後期 理学研究科 2019/04-2020/03
有機金属化学論 Organometallic Chemistry 後期 理学研究科 2019/04-2020/03
現代有機化学論 Topics in Current Organic Chemistry 後期 理学研究科 2019/04-2020/03

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Faculty management (title, position)
Title Period
理学研究科国際・社会交流・広報委員会委員 2018/04/01-2019/03/31
理学研究科国際・社会交流・広報委員会 社会交流小委員会委員 2018/04/01-2019/03/31
理学研究科国際・社会交流・広報委員会 社会交流小委員会 社会交流室・ELCASワーキンググループ 2018/04/01-2019/03/31
2019/04/01-2020/03/31
理学研究科SACRA広報・社会連携部門委員会 社会連携小委員会委員 2019/04/01-2020/03/31