Yanagi, M.; Ueda, Y.; Ninomiya, R.; Imayoshi, A.; Furuta, T.; Mishiro, K.; Kawabata, T. |
Yanagi, M.; Ueda, Y.; Ninomiya, R.; Imayoshi, A.; Furuta, T.; Mishiro, K.; Kawabata, T. |
Yanagi, M.; Ueda, Y.; Ninomiya, R.; Imayoshi, A.; Furuta, T.; Mishiro, K.; Kawabata, T. |
Synthesis of 4-Deoxy Pyranosides via Catalyst-Controlled Site-Selective Toluoylation of Abundant Sugars |
Synthesis of 4-Deoxy Pyranosides via Catalyst-Controlled Site-Selective Toluoylation of Abundant Sugars |
Synthesis of 4-Deoxy Pyranosides via Catalyst-Controlled Site-Selective Toluoylation of Abundant Sugars |
Organic Letters, 21, 13, 5006-5009 |
Organic Letters, 21, 13, 5006-5009 |
Organic Letters, 21, 13, 5006-5009 |
2019/06 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Kawabata, T. |
川端 猛夫 |
Kawabata, T. |
Potential in Acylation |
感動の瞬間:アシル化を通して見えるもの |
Potential in Acylation |
Journal of Synthetic Organic Chemistry, Japan, 77, 3, 268-271 |
有機合成化学協会誌, 77, 3, 268-271 |
Journal of Synthetic Organic Chemistry, Japan, 77, 3, 268-271 |
2019/03 |
Refereed |
Japanese |
Research paper(scientific journal) |
Disclose to all |
Irie, Y.; Hanaki, M.; Murakami, K.; Imamoto, T.; Furuta, T.; Kawabata, T.; Kawase, T.; Hirose, K.; Minobe, Y.; Akagi, K.; Yanagita, R. C.; Irie, K. |
Irie, Y.; Hanaki, M.; Murakami, K.; Imamoto, T.; Furuta, T.; Kawabata, T.; Kawase, T.; Hirose, K.; Minobe, Y.; Akagi, K.; Yanagita, R. C.; Irie, K. |
Irie, Y.; Hanaki, M.; Murakami, K.; Imamoto, T.; Furuta, T.; Kawabata, T.; Kawase, T.; Hirose, K.; Minobe, Y.; Akagi, K.; Yanagita, R. C.; Irie, K. |
Synthesis and biochemical characterization of quasi-stable trimer models of full-length amyloid β40 with a toxic conformation |
Synthesis and biochemical characterization of quasi-stable trimer models of full-length amyloid β40 with a toxic conformation |
Synthesis and biochemical characterization of quasi-stable trimer models of full-length amyloid β40 with a toxic conformation |
Chemical Communications, 55, 2, 182-185 |
Chemical Communications, 55, 2, 182-185 |
Chemical Communications, 55, 2, 182-185 |
2018/11 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Murai, T.; Xing, Y.; Kuribayashi, T.; Lu, W.; Guo, J.; Yella, R.; Hamada, S.; Sasamori, T.; Tokitoh, N.; Kawabata, T.; Furuta, T. |
Murai, T.; Xing, Y.; Kuribayashi, T.; Lu, W.; Guo, J.; Yella, R.; Hamada, S.; Sasamori, T.; Tokitoh, N.; Kawabata, T.; Furuta, T. |
Murai, T.; Xing, Y.; Kuribayashi, T.; Lu, W.; Guo, J.; Yella, R.; Hamada, S.; Sasamori, T.; Tokitoh, N.; Kawabata, T.; Furuta, T. |
Synthesis and Structural properties of Axially Chiral Binaphthothiophene Dicarboxylic Acid |
Synthesis and Structural properties of Axially Chiral Binaphthothiophene Dicarboxylic Acid |
Synthesis and Structural properties of Axially Chiral Binaphthothiophene Dicarboxylic Acid |
Chemical and Pharmaceutical Bulletein, 66, 12, 1203-1206 |
Chemical and Pharmaceutical Bulletein, 66, 12, 1203-1206 |
Chemical and Pharmaceutical Bulletein, 66, 12, 1203-1206 |
2018/10 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Hyakutake, R.; Yoshimura, T.; Ueda, Y.; Hayashi, K.; Furuta, T.; Kawabata, T. |
Hyakutake, R.; Yoshimura, T.; Ueda, Y.; Hayashi, K.; Furuta, T.; Kawabata, T. |
Hyakutake, R.; Yoshimura, T.; Ueda, Y.; Hayashi, K.; Furuta, T.; Kawabata, T. |
Asymmetric Synthesis of ß-Lactams by Intramolecular Conjugate Addition of Serine and Cysteine Derivatives via Memory of Chirality |
Asymmetric Synthesis of ß-Lactams by Intramolecular Conjugate Addition of Serine and Cysteine Derivatives via Memory of Chirality |
Asymmetric Synthesis of ß-Lactams by Intramolecular Conjugate Addition of Serine and Cysteine Derivatives via Memory of Chirality |
Heterocycles, 97, 2, 1128-1147 |
Heterocycles, 97, 2, 1128-1147 |
Heterocycles, 97, 2, 1128-1147 |
2018/06 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Arai, K.; Ueda, Y.; Morisaki, K.; Furuta, T.; Sasamori, T.; Tokitoh, N.; Kawabata, T. |
Arai, K.; Ueda, Y.; Morisaki, K.; Furuta, T.; Sasamori, T.; Tokitoh, N.; Kawabata, T. |
Arai, K.; Ueda, Y.; Morisaki, K.; Furuta, T.; Sasamori, T.; Tokitoh, N.; Kawabata, T. |
Intermolecular Chemo- and Regioselective Aromatic C-H Amination of Alkoxyarenes Promoted by Rhodium Nitrenoids |
Intermolecular Chemo- and Regioselective Aromatic C-H Amination of Alkoxyarenes Promoted by Rhodium Nitrenoids |
Intermolecular Chemo- and Regioselective Aromatic C-H Amination of Alkoxyarenes Promoted by Rhodium Nitrenoids |
Chemical Communications, 54, 18, 2264-2267 |
Chemical Communications, 54, 18, 2264-2267 |
Chemical Communications, 54, 18, 2264-2267 |
2018/03 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Ohtsuki, H.; Takashima, M.; Furuta, T.; Kawabata, T. |
Ohtsuki, H.; Takashima, M.; Furuta, T.; Kawabata, T. |
Ohtsuki, H.; Takashima, M.; Furuta, T.; Kawabata, T. |
Direct Asymmetric Synthesis of a-Deuterated a-Amino Acid Derivatives from the Parent a-Amino Acid via Memory of Chirality |
Direct Asymmetric Synthesis of a-Deuterated a-Amino Acid Derivatives from the Parent a-Amino Acid via Memory of Chirality |
Direct Asymmetric Synthesis of a-Deuterated a-Amino Acid Derivatives from the Parent a-Amino Acid via Memory of Chirality |
Tetrahedron Letters, 59, 13, 1188-1191 |
Tetrahedron Letters, 59, 13, 1188-1191 |
Tetrahedron Letters, 59, 13, 1188-1191 |
2018/03 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Nobuta T.; Kawabata T. |
Nobuta T.; Kawabata T. |
Nobuta T.; Kawabata T. |
Catalyst-Controlled Site-Selective Asymmetric Epoxidation of Nerylamine and Geranylamine Derivatives |
Catalyst-Controlled Site-Selective Asymmetric Epoxidation of Nerylamine and Geranylamine Derivatives |
Catalyst-Controlled Site-Selective Asymmetric Epoxidation of Nerylamine and Geranylamine Derivatives |
Chemical Communications, 53, 67, 9320-9323 |
Chemical Communications, 53, 67, 9320-9323 |
Chemical Communications, 53, 67, 9320-9323 |
2017/08 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Yanagi, M.; Imayoshi, A.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Yanagi, M.; Imayoshi, A.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Yanagi, M.; Imayoshi, A.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Carboxylate Anions Accelerate Pyrrolidinopyridine (PPy)-Catalyzed Acylation: Catalytic Site-Selective Acylation of a Carbohydrate in Situ Counteranion Exchange |
Carboxylate Anions Accelerate Pyrrolidinopyridine (PPy)-Catalyzed Acylation: Catalytic Site-Selective Acylation of a Carbohydrate in Situ Counteranion Exchange |
Carboxylate Anions Accelerate Pyrrolidinopyridine (PPy)-Catalyzed Acylation: Catalytic Site-Selective Acylation of a Carbohydrate in Situ Counteranion Exchange |
Organic Letters, 19, 12, 3099-3012 |
Organic Letters, 19, 12, 3099-3012 |
Organic Letters, 19, 12, 3099-3012 |
2017/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Yoshida, K.; Hirata, A.; Hashimoto, H.; Imayoshi, A.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Yoshida, K.; Hirata, A.; Hashimoto, H.; Imayoshi, A.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Yoshida, K.; Hirata, A.; Hashimoto, H.; Imayoshi, A.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Organocatalytic Chemoselective Monoacylation of 1,n-Linear Disulfonamides |
Organocatalytic Chemoselective Monoacylation of 1,n-Linear Disulfonamides |
Organocatalytic Chemoselective Monoacylation of 1,n-Linear Disulfonamides |
Tetrahedron Letters, 58, 11, 1030-1033 |
Tetrahedron Letters, 58, 11, 1030-1033 |
Tetrahedron Letters, 58, 11, 1030-1033 |
2017/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Takeuchi, H.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Takeuchi, H.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Takeuchi, H.; Ueda, Y.; Furuta, T.; Kawabata, T. |
Total Synthesis of Ellagitannins via Sequential Site-Selective Functionalization of Unprotected D-Glucose |
Total Synthesis of Ellagitannins via Sequential Site-Selective Functionalization of Unprotected D-Glucose |
Total Synthesis of Ellagitannins via Sequential Site-Selective Functionalization of Unprotected D-Glucose |
Chemical and Pharmaceutical Bulletin, 65, 1, 25-32 |
Chemical and Pharmaceutical Bulletin, 65, 1, 25-32 |
Chemical and Pharmaceutical Bulletin, 65, 1, 25-32 |
2017/01 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Kasamatsu, K.; Yoshimura, T.; Mandi, A.; Taniguchi, T.; Monde, K.; Furuta, T.; Kawabata, T. |
Kasamatsu, K.; Yoshimura, T.; Mandi, A.; Taniguchi, T.; Monde, K.; Furuta, T.; Kawabata, T. |
Kasamatsu, K.; Yoshimura, T.; Mandi, A.; Taniguchi, T.; Monde, K.; Furuta, T.; Kawabata, T. |
α-Arylation of α-Amino Acid Derivatives with Arynes via Memory of Chirality: Asymmetric Synthesis of Benzocyclobutenones with Tetrasubstituted Carbon |
α-Arylation of α-Amino Acid Derivatives with Arynes via Memory of Chirality: Asymmetric Synthesis of Benzocyclobutenones with Tetrasubstituted Carbon |
α-Arylation of α-Amino Acid Derivatives with Arynes via Memory of Chirality: Asymmetric Synthesis of Benzocyclobutenones with Tetrasubstituted Carbon |
Organic Letters, 19, 2, 352-355 |
Organic Letters, 19, 2, 352-355 |
Organic Letters, 19, 2, 352-355 |
2017/01 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Lu, W.; Pei, X.;Murai, T.; Sasamori, T.; Tlkitoh, N.; Kawabata, T.; Furuta, T. |
Lu, W.; Pei, X.;Murai, T.; Sasamori, T.; Tlkitoh, N.; Kawabata, T.; Furuta, T. |
Lu, W.; Pei, X.;Murai, T.; Sasamori, T.; Tlkitoh, N.; Kawabata, T.; Furuta, T. |
Asymmetric Intramolecular C-H Insertion Promoted by Dirhodium(II) Carboxylate Catalyst Bearing Axially Chiral Amino Acid Derivatives |
Asymmetric Intramolecular C-H Insertion Promoted by Dirhodium(II) Carboxylate Catalyst Bearing Axially Chiral Amino Acid Derivatives |
Asymmetric Intramolecular C-H Insertion Promoted by Dirhodium(II) Carboxylate Catalyst Bearing Axially Chiral Amino Acid Derivatives |
Synlett, 28, 679-683 |
Synlett, 28, 679-683 |
Synlett, 28, 679-683 |
2017 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Yanagi, M.; Ninomiya, R.; Ueda, Y.; Furuta, T.; Yamada, T.; Sunazuka, T.; Kawabata, T. |
Yanagi, M.; Ninomiya, R.; Ueda, Y.; Furuta, T.; Yamada, T.; Sunazuka, T.; Kawabata, T. |
Yanagi, M.; Ninomiya, R.; Ueda, Y.; Furuta, T.; Yamada, T.; Sunazuka, T.; Kawabata, T. |
Organocatalytic Site-Selective Acylation of 10-Deacetylbaccatin III |
Organocatalytic Site-Selective Acylation of 10-Deacetylbaccatin III |
Organocatalytic Site-Selective Acylation of 10-Deacetylbaccatin III |
Chemical and Pharmaceutical Bulletin, 64, 7, 907-912 |
Chemical and Pharmaceutical Bulletin, 64, 7, 907-912 |
Chemical and Pharmaceutical Bulletin, 64, 7, 907-912 |
2016/07 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Mishiro, K.; Takeuchi, H.; Furuta, T.; Kawabta, T. |
Mishiro, K.; Takeuchi, H.; Furuta, T.; Kawabta, T. |
Mishiro, K.; Takeuchi, H.; Furuta, T.; Kawabta, T. |
A Concise Access to C2-Symmetric Chiral 4-Pyrrolidinopyridine Catalysts with Dual Functional Side Chains |
A Concise Access to C2-Symmetric Chiral 4-Pyrrolidinopyridine Catalysts with Dual Functional Side Chains |
A Concise Access to C2-Symmetric Chiral 4-Pyrrolidinopyridine Catalysts with Dual Functional Side Chains |
Chemical and Pharmaceutical Bulletin, 64, 7, 1073-1077 |
Chemical and Pharmaceutical Bulletin, 64, 7, 1073-1077 |
Chemical and Pharmaceutical Bulletin, 64, 7, 1073-1077 |
2016/07 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Yamada, T.; Suzuki, K.; Hirose, T.; Furuta, T.; Ueda, Y.; Kawabata, T.; Omura, S.; Sunazuka, T. |
Yamada, T.; Suzuki, K.; Hirose, T.; Furuta, T.; Ueda, Y.; Kawabata, T.; Omura, S.; Sunazuka, T. |
Yamada, T.; Suzuki, K.; Hirose, T.; Furuta, T.; Ueda, Y.; Kawabata, T.; Omura, S.; Sunazuka, T. |
Organocatalytic Site-Selective Acylation of Avermect in B2a, a Unique Endectocidal Drug |
Organocatalytic Site-Selective Acylation of Avermectin B2a, a Unique Endectocidal Drug |
Organocatalytic Site-Selective Acylation of Avermect in B2a, a Unique Endectocidal Drug |
Chemical and Pharmaceutical Bulletin, 64, 7, 856-864 |
Chemical and Pharmaceutical Bulletin, 64, 7, 856-864 |
Chemical and Pharmaceutical Bulletin, 64, 7, 856-864 |
2016/07 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Tomohara, K.; Kasamatsu, K.; Yoshimura, T.; Furuta, T.; Kawabata, T. |
Tomohara, K.; Kasamatsu, K.; Yoshimura, T.; Furuta, T.; Kawabata, T. |
Tomohara, K.; Kasamatsu, K.; Yoshimura, T.; Furuta, T.; Kawabata, T. |
Asymmetric Synthesis of Multisubstituted Dihydrobenzofurans by Intramolecular Conjugate Addition of Short-Lived C-O Axially Chiral Enolates |
Asymmetric Synthesis of Multisubstituted Dihydrobenzofurans by Intramolecular Conjugate Addition of Short-Lived C-O Axially Chiral Enolates |
Asymmetric Synthesis of Multisubstituted Dihydrobenzofurans by Intramolecular Conjugate Addition of Short-Lived C-O Axially Chiral Enolates |
Chemical and Pharmaceutical Bulletin, 64, 7, 899-906 |
Chemical and Pharmaceutical Bulletin, 64, 7, 899-906 |
Chemical and Pharmaceutical Bulletin, 64, 7, 899-906 |
2016/07 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Alezra, V. ; Kawabata, T. |
Alezra, V. ; Kawabata, T. |
Alezra, V. ; Kawabata, T. |
Recent Progress in Memory Of Chirality (MOC) : An Advanced Chiral Pool |
Recent Progress in Memory Of Chirality (MOC) : An Advanced Chiral Pool |
Recent Progress in Memory Of Chirality (MOC) : An Advanced Chiral Pool |
Synthesis, 48, 18, 2997-3016 |
Synthesis, 48, 18, 2997-3016 |
Synthesis, 48, 18, 2997-3016 |
2016/07 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Imayoshi, A.; Yamanaka, M.; Sato, M.; Yoshida, K.; Furuta, T.; Ueda, Y.; Kawabata, T. |
Imayoshi, A.; Yamanaka, M.; Sato, M.; Yoshida, K.; Furuta, T.; Ueda, Y.; Kawabata, T. |
Imayoshi, A.; Yamanaka, M.; Sato, M.; Yoshida, K.; Furuta, T.; Ueda, Y.; Kawabata, T. |
Insights into the Molecular Recognition Process in Organocatalytic Chemoselective Monoacylation of 1,5-Pentanediol |
Insights into the Molecular Recognition Process in Organocatalytic Chemoselective Monoacylation of 1,5-Pentanediol |
Insights into the Molecular Recognition Process in Organocatalytic Chemoselective Monoacylation of 1,5-Pentanediol |
Advanced Synthesis & Catalysis, 358, 8, 1337-1344 |
Advanced Synthesis & Catalysis, 358, 8, 1337-1344 |
Advanced Synthesis & Catalysis, 358, 8, 1337-1344 |
2016/04 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Hyakutake, R.; Gondo, N.; Ueda, Y.; Yoshimura, T.; Furuta, T.; Kawabata, T. |
Hyakutake, R.; Gondo, N.; Ueda, Y.; Yoshimura, T.; Furuta, T.; Kawabata, T. |
Hyakutake, R.; Gondo, N.; Ueda, Y.; Yoshimura, T.; Furuta, T.; Kawabata, T. |
Catalyst-Controlled Regiodivergent Vinylogous Aza-Morita-Baylis-Hillman Reactions |
Catalyst-Controlled Regiodivergent Vinylogous Aza-Morita-Baylis-Hillman Reactions |
Catalyst-Controlled Regiodivergent Vinylogous Aza-Morita-Baylis-Hillman Reactions |
Tetrahedron Letters, 57, 12, 1321-1324 |
Tetrahedron Letters, 57, 12, 1321-1324 |
Tetrahedron Letters, 57, 12, 1321-1324 |
2016/03 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Baba, T.; Yamamoto, J.; Hayashi, K.; Sato, M.; Yamanaka, M.; Kawabata, T.; Furuta, T. |
Baba, T.; Yamamoto, J.; Hayashi, K.; Sato, M.; Yamanaka, M.; Kawabata, T.; Furuta, T. |
Baba, T.; Yamamoto, J.; Hayashi, K.; Sato, M.; Yamanaka, M.; Kawabata, T.; Furuta, T. |
Catalytic Discrimination Among Formyl Groups in Regio- and Stereoselective Intramolecular Cross-Aldol Reactions  |
Catalytic Discrimination Among Formyl Groups in Regio- and Stereoselective Intramolecular Cross-Aldol Reactions  |
Catalytic Discrimination Among Formyl Groups in Regio- and Stereoselective Intramolecular Cross-Aldol Reactions  |
Chem. Science, 7, 6, 3791-3797 |
Chem. Science, 7, 6, 3791-3797 |
Chem. Science, 7, 6, 3791-3797 |
2016/02 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Y. Ueda; T. Furuta; T. Kawabata |
Y. Ueda; T. Furuta; T. Kawabata |
Y. Ueda; T. Furuta; T. Kawabata |
Final-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A–C  |
Final-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A–C  |
Final-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A–C  |
Angewandte Chemie International Edition, 54, 41, 11966-11970 |
Angewandte Chemie International Edition, 54, 41, 11966-11970 |
Angewandte Chemie International Edition, 54, 41, 11966-11970 |
2015/10 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
H. Takeuchi; K. Mishiro; Y. Ueda; Y. Fujimori; T. Firita; T. Kawabata |
H. Takeuchi; K. Mishiro; Y. Ueda; Y. Fujimori; T. Firita; T. Kawabata |
H. Takeuchi; K. Mishiro; Y. Ueda; Y. Fujimori; T. Firita; T. Kawabata |
Total Synthesis of Ellagitannins through Regioselective Sequential Functionalization of Unprotected Glucose  |
Total Synthesis of Ellagitannins through Regioselective Sequential Functionalization of Unprotected Glucose  |
Total Synthesis of Ellagitannins through Regioselective Sequential Functionalization of Unprotected Glucose  |
Angewandte Chemie, 54, 21, 6177-6180 |
Angewandte Chemie, 54, 21, 6177-6180 |
Angewandte Chemie, 54, 21, 6177-6180 |
2015/04 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
M. Yamanaka; U. Yoshida; M. Sato; T. Shigeta; K. Yoshida; T. Furuta; T. Kawabata |
M. Yamanaka; U. Yoshida; M. Sato; T. Shigeta; K. Yoshida; T. Furuta; T. Kawabata |
M. Yamanaka; U. Yoshida; M. Sato; T. Shigeta; K. Yoshida; T. Furuta; T. Kawabata |
Origin of High E-Selectivity in 4-Pyrrolidinopyridine-Catalyzed Tetrasubstituted α,α′-Alkenediol: A Computational and Experimental Study |
Origin of High E-Selectivity in 4-Pyrrolidinopyridine-Catalyzed Tetrasubstituted α,α′-Alkenediol: A Computational and Experimental Study |
Origin of High E-Selectivity in 4-Pyrrolidinopyridine-Catalyzed Tetrasubstituted α,α′-Alkenediol: A Computational and Experimental Study |
Journal of Organic Chemistry, 80, 6, 3075-3082 |
Journal of Organic Chemistry, 80, 6, 3075-3082 |
Journal of Organic Chemistry, 80, 6, 3075-3082 |
2015/02 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
川端 猛夫 |
川端 猛夫 |
|
アシル化触媒 |
アシル化触媒 |
|
月刊ファインケミカル, 43, 6, 14-23 |
月刊ファインケミカル, 43, 6, 14-23 |
, 43, 6, 14-23 |
2014/06 |
|
Japanese |
Research paper(other science council materials etc.) |
Disclose to all |
K. Nakanishi; D. Fukatsu; K. Takaishi; T. Tsuji; K. Kuramochi; T. Kawabata; K. Tsubaki |
K. Nakanishi; D. Fukatsu; K. Takaishi; T. Tsuji; K. Kuramochi; T. Kawabata; K. Tsubaki |
K. Nakanishi; D. Fukatsu; K. Takaishi; T. Tsuji; K. Kuramochi; T. Kawabata; K. Tsubaki |
Oligonaphthofurans: Fan-Shaped and Three-Dimensional π-Compounds |
Oligonaphthofurans: Fan-Shaped and Three-Dimensional π-Compounds |
Oligonaphthofurans: Fan-Shaped and Three-Dimensional π-Compounds |
Journal of the American Chemical Society, 136, 19, 7101-7109 |
Journal of the American Chemical Society, 136, 19, 7101-7109 |
Journal of the American Chemical Society, 136, 19, 7101-7109 |
2014/04 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
S. Hamada; Y. Wada; T. Sasamori; N. Tokitoh; T. Furura; T. Kawabata |
S. Hamada; Y. Wada; T. Sasamori; N. Tokitoh; T. Furura; T. Kawabata |
S. Hamada; Y. Wada; T. Sasamori; N. Tokitoh; T. Furura; T. Kawabata |
Oxidative kinetic resolution of racemic alkyl aryl carbinols by an electronically tuned chiral nitroxyl radical  |
Oxidative kinetic resolution of racemic alkyl aryl carbinols by an electronically tuned chiral nitroxyl radical  |
Oxidative kinetic resolution of racemic alkyl aryl carbinols by an electronically tuned chiral nitroxyl radical  |
Tetrahedron Letters, 55, 11, 1943-1945 |
Tetrahedron Letters, 55, 11, 1943-1945 |
Tetrahedron Letters, 55, 11, 1943-1945 |
2014/03 |
Refereed |
English |
|
Disclose to all |
K. Nakanishi; T. Sasamori; K. Kuromochi, N. Tokitoh; T. Kabata; K. Tsubaki |
K. Nakanishi; T. Sasamori; K. Kuromochi, N. Tokitoh; T. Kabata; K. Tsubaki |
K. Nakanishi; T. Sasamori; K. Kuromochi, N. Tokitoh; T. Kabata; K. Tsubaki |
Synthesis and Properties of Butterfly-Shaped Expanded Naphthofuran Derivatives |
Synthesis and Properties of Butterfly-Shaped Expanded Naphthofuran Derivatives |
Synthesis and Properties of Butterfly-Shaped Expanded Naphthofuran Derivatives |
Journal of Organic Chemistry, 79, 6, 2625-2631 |
Journal of Organic Chemistry, 79, 6, 2625-2631 |
Journal of Organic Chemistry, 79, 6, 2625-2631 |
2014/02 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
K. Mishiro; T. Furuta; T. Sasamori; K. Hayashi; N. Tokitoh; S. Futaki; T. Kawabata |
K. Mishiro; T. Furuta; T. Sasamori; K. Hayashi; N. Tokitoh; S. Futaki; T. Kawabata |
K. Mishiro; T. Furuta; T. Sasamori; K. Hayashi; N. Tokitoh; S. Futaki; T. Kawabata |
A cyclochiral conformational motif constructed using a robust hydrogen-bonding network |
A cyclochiral conformational motif constructed using a robust hydrogen-bonding network |
A cyclochiral conformational motif constructed using a robust hydrogen-bonding network |
Journal of the American Chemical Society, 135, 37, 13644-13647 |
Journal of the American Chemical Society, 135, 37, 13644-13647 |
Journal of the American Chemical Society, 135, 37, 13644-13647 |
2013/09 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
K. Tomohara; T. Yoshimura; R. Hyakutake; P. Yang; T. Kawabata |
K. Tomohara; T. Yoshimura; R. Hyakutake; P. Yang; T. Kawabata |
K. Tomohara; T. Yoshimura; R. Hyakutake; P. Yang; T. Kawabata |
Asymmetric α-arylation of amino acid derivatives by clayden rearrangement of ester enolates via memory of chirality |
Asymmetric α-arylation of amino acid derivatives by clayden rearrangement of ester enolates via memory of chirality |
Asymmetric α-arylation of amino acid derivatives by clayden rearrangement of ester enolates via memory of chirality |
Journal of the American Chemical Society, 135, 36, 13294-13297 |
Journal of the American Chemical Society, 135, 36, 13294-13297 |
Journal of the American Chemical Society, 135, 36, 13294-13297 |
2013/08 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
S. Hamada; T. Furuta; Y. Wada; T. Kawabata |
S. Hamada; T. Furuta; Y. Wada; T. Kawabata |
S. Hamada; T. Furuta; Y. Wada; T. Kawabata |
Chemoselective oxidation by electronically tuned nitroxyl radical catalysts |
Chemoselective oxidation by electronically tuned nitroxyl radical catalysts |
Chemoselective oxidation by electronically tuned nitroxyl radical catalysts |
Angewandte Chemie - International Edition, 52, 31, 8093-8097 |
Angewandte Chemie - International Edition, 52, 31, 8093-8097 |
Angewandte Chemie - International Edition, 52, 31, 8093-8097 |
2013/07/29 |
Refereed |
English |
|
Disclose to all |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Angewandte Chemie, 52, 25, 6445-6449 |
Angewandte Chemie, 52, 25, 6445-6449 |
Angewandte Chemie, 52, 25, 6445-6449 |
2013/06 |
Refereed |
English |
|
Disclose to all |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Angewandte Chemie, 52, 25, 6445-6449 |
Angewandte Chemie, 52, 25, 6445-6449 |
Angewandte Chemie, 52, 25, 6445-6449 |
2013/06 |
Refereed |
English |
|
Disclose to all |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
R. Nishino; T. Furuta; K. Kan; M. Sato; M. Yamanaka; T. Sasamori; N. Tokitoh; T. Kawabata |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate |
Angewandte Chemie, 52, 25, 6445-6449 |
Angewandte Chemie, 52, 25, 6445-6449 |
Angewandte Chemie, 52, 25, 6445-6449 |
2013/06 |
Refereed |
English |
|
Disclose to all |
T. Yoshimura; K. Tomohara; T. Kawabata |
T. Yoshimura; K. Tomohara; T. Kawabata |
T. Yoshimura; K. Tomohara; T. Kawabata |
Asymmetric induction via short-lived chiral enolates with a chiral C-O axis |
Asymmetric induction via short-lived chiral enolates with a chiral C-O axis |
Asymmetric induction via short-lived chiral enolates with a chiral C-O axis |
Journal of the American Chemical Society, 135, 19, 7102-7105 |
Journal of the American Chemical Society, 135, 19, 7102-7105 |
Journal of the American Chemical Society, 135, 19, 7102-7105 |
2013/05/15 |
Refereed |
English |
|
Disclose to all |
T. Furuta; M. Nikaido; J. Yamamoto; T. Kuribayashi; T. Kawabata |
T. Furuta; M. Nikaido; J. Yamamoto; T. Kuribayashi; T. Kawabata |
T. Furuta; M. Nikaido; J. Yamamoto; T. Kuribayashi; T. Kawabata |
Synthesis of axially chiral amino acid derivatives via the selective monoesterification of 1,1′-biaryl-2,2′-dicarboxylic acids |
Synthesis of axially chiral amino acid derivatives via the selective monoesterification of 1,1′-biaryl-2,2′-dicarboxylic acids |
Synthesis of axially chiral amino acid derivatives via the selective monoesterification of 1,1′-biaryl-2,2′-dicarboxylic acids |
Synthesis (Germany), 45, 10, 1312-1318 |
Synthesis (Germany), 45, 10, 1312-1318 |
Synthesis (Germany), 45, 10, 1312-1318 |
2013/05 |
Refereed |
English |
|
Disclose to all |
T. Yoshimura; T. Kinoshita; H. Yoshioka; T. Kawabata |
T. Yoshimura; T. Kinoshita; H. Yoshioka; T. Kawabata |
T. Yoshimura; T. Kinoshita; H. Yoshioka; T. Kawabata |
Asymmetric intermolecular conjugate addition of amino acid derivatives via memory of chirality: Total synthesis of manzacidin A |
Asymmetric intermolecular conjugate addition of amino acid derivatives via memory of chirality: Total synthesis of manzacidin A |
Asymmetric intermolecular conjugate addition of amino acid derivatives via memory of chirality: Total synthesis of manzacidin A |
Organic Letters, 15, 4, 864-867 |
Organic Letters, 15, 4, 864-867 |
Organic Letters, 15, 4, 864-867 |
2013/02/15 |
Refereed |
English |
|
Disclose to all |
D. Monguchi; T. Yoshimura; K. Irie; K. Hayashi; S. Majumdar; T. Sasamori; N. Tokitoh; T. Kawabata |
D. Monguchi; T. Yoshimura; K. Irie; K. Hayashi; S. Majumdar; T. Sasamori; N. Tokitoh; T. Kawabata |
D. Monguchi; T. Yoshimura; K. Irie; K. Hayashi; S. Majumdar; T. Sasamori; N. Tokitoh; T. Kawabata |
Asymmetric intramolecular conjugate addition of α-amino acid derivatives via racemization-free equilibrium of intermediary chiral enolates |
Asymmetric intramolecular conjugate addition of α-amino acid derivatives via racemization-free equilibrium of intermediary chiral enolates |
Asymmetric intramolecular conjugate addition of α-amino acid derivatives via racemization-free equilibrium of intermediary chiral enolates |
Heterocycles, 86, 2, 1483-1494 |
Heterocycles, 86, 2, 1483-1494 |
Heterocycles, 86, 2, 1483-1494 |
2012/12/31 |
Refereed |
English |
|
Disclose to all |
T. Yoshimura; M. Takuwa; K. Tomohara; M. Uyama; K. Hayashi; P. Yang; R. Hyakutake; T. Sasamori; N. Tokitoh; T. Kawabata |
T. Yoshimura; M. Takuwa; K. Tomohara; M. Uyama; K. Hayashi; P. Yang; R. Hyakutake; T. Sasamori; N. Tokitoh; T. Kawabata |
T. Yoshimura; M. Takuwa; K. Tomohara; M. Uyama; K. Hayashi; P. Yang; R. Hyakutake; T. Sasamori; N. Tokitoh; T. Kawabata |
Protonation-assisted conjugate addition of axially chiral enolates: Asymmetric synthesis of multisubstituted β-lactams from α-amino acids |
Protonation-assisted conjugate addition of axially chiral enolates: Asymmetric synthesis of multisubstituted β-lactams from α-amino acids |
Protonation-assisted conjugate addition of axially chiral enolates: Asymmetric synthesis of multisubstituted β-lactams from α-amino acids |
Chemistry - A European Journal, 18, 48, 15330-15336 |
Chemistry - A European Journal, 18, 48, 15330-15336 |
Chemistry - A European Journal, 18, 48, 15330-15336 |
2012/11 |
Refereed |
English |
|
Disclose to all |
K. Yoshida; K. Mishiro; Y. Ueda; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; K. Mishiro; Y. Ueda; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; K. Mishiro; Y. Ueda; T. Shigeta; T. Furuta; T. Kawabata |
Non-enzymatic geometry-selective acylation of tri- and tetrasubstituted α,α\\'-alkenediols |
Non-enzymatic geometry-selective acylation of tri- and tetrasubstituted α,α\\'-alkenediols |
Non-enzymatic geometry-selective acylation of tri- and tetrasubstituted α,α\\'-alkenediols |
Advanced Synthesis and Catalysis, 354, 17, 3291-3298 |
Advanced Synthesis and Catalysis, 354, 17, 3291-3298 |
Advanced Synthesis and Catalysis, 354, 17, 3291-3298 |
2012/11 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
H. Schedel; K. Kan; Y. Ueda; K. Mishiro; K. Yoshida; T. Furuta; T. Kawabata |
H. Schedel; K. Kan; Y. Ueda; K. Mishiro; K. Yoshida; T. Furuta; T. Kawabata |
H. Schedel; K. Kan; Y. Ueda; K. Mishiro; K. Yoshida; T. Furuta; T. Kawabata |
Asymmetric desymmetrization of meso-diols by C <sub>2</sub>-symmetric chiral 4-pyrrolidinopyridines  |
Asymmetric desymmetrization of meso-diols by C <sub>2</sub>-symmetric chiral 4-pyrrolidinopyridines  |
Asymmetric desymmetrization of meso-diols by C <sub>2</sub>-symmetric chiral 4-pyrrolidinopyridines  |
Beilstein Journal of Organic Chemistry, 8, 1778-1787 |
Beilstein Journal of Organic Chemistry, 8, 1778-1787 |
Beilstein Journal of Organic Chemistry, 8, 1778-1787 |
2012/10/17 |
Refereed |
English |
|
Disclose to all |
Y. Ueda; K. Mishiro; K. Yoshida; T. Furuta; T. Kawabata |
Y. Ueda; K. Mishiro; K. Yoshida; T. Furuta; T. Kawabata |
Y. Ueda; K. Mishiro; K. Yoshida; T. Furuta; T. Kawabata |
Regioselective diversification of a cardiac glycoside, lanatoside C, by organocatalysis |
Regioselective diversification of a cardiac glycoside, lanatoside C, by organocatalysis |
Regioselective diversification of a cardiac glycoside, lanatoside C, by organocatalysis |
Journal of Organic Chemistry, 77, 18, 7850-7857 |
Journal of Organic Chemistry, 77, 18, 7850-7857 |
Journal of Organic Chemistry, 77, 18, 7850-7857 |
2012/09/21 |
Refereed |
English |
|
Disclose to all |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Chemical Communications, 48, 55, 6981-6983 |
Chemical Communications, 48, 55, 6981-6983 |
Chemical Communications, 48, 55, 6981-6983 |
2012/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
T. Furuta; T. Kawabata |
T. Furuta; T. Kawabata |
T. Furuta; T. Kawabata |
Chiral DMAP-Type Catalysts for Acyl-Transfer Reactions |
Chiral DMAP-Type Catalysts for Acyl-Transfer Reactions |
Chiral DMAP-Type Catalysts for Acyl-Transfer Reactions |
Science of Synthesis, Asymmetric Organocatalysis 1, Lewis Base and Acid Catalysts, 497-546 |
Science of Synthesis, Asymmetric Organocatalysis 1, Lewis Base and Acid Catalysts, 497-546 |
Science of Synthesis, Asymmetric Organocatalysis 1, Lewis Base and Acid Catalysts, 497-546 |
2012/05 |
Refereed |
English |
|
Disclose to all |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Chemical Communications, 48, 55, 6981-6983 |
Chemical Communications, 48, 55, 6981-6983 |
Chemical Communications, 48, 55, 6981-6983 |
2012/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
K. Yoshida; T. Shigeta; T. Furuta; T. Kawabata |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives  |
Chemical Communications, 48, 55, 6981-6983 |
Chemical Communications, 48, 55, 6981-6983 |
Chemical Communications, 48, 55, 6981-6983 |
2012/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
H. Watanabe; T. Yoshimura; S. Kawakami; T. Sasamori; N. Tokitoh; T. Kawabata |
H. Watanabe; T. Yoshimura; S. Kawakami; T. Sasamori; N. Tokitoh; T. Kawabata |
H. Watanabe; T. Yoshimura; S. Kawakami; T. Sasamori; N. Tokitoh; T. Kawabata |
Asymmetric aldol reaction via memory of chirality  |
Asymmetric aldol reaction via memory of chirality  |
Asymmetric aldol reaction via memory of chirality  |
Chemical Communications, 48, 43, 5346-5348 |
Chemical Communications, 48, 43, 5346-5348 |
Chemical Communications, 48, 43, 5346-5348 |
2012/04 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
Y. Azuma; H. Imai; T. Yoshimura; T. Kawabata; M. Imanishi; S. Futaki |
Y. Azuma; H. Imai; T. Yoshimura; T. Kawabata; M. Imanishi; S. Futaki |
Y. Azuma; H. Imai; T. Yoshimura; T. Kawabata; M. Imanishi; S. Futaki |
Dipicolylamine as a unique structural switching element for helical peptides |
Dipicolylamine as a unique structural switching element for helical peptides |
Dipicolylamine as a unique structural switching element for helical peptides |
Organic and Biomolecular Chemistry, 10, 30, 6062-6068 |
Organic and Biomolecular Chemistry, 10, 30, 6062-6068 |
Organic and Biomolecular Chemistry, 10, 30, 6062-6068 |
2012/04 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
2011/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
F. Teraoka; K. Fuji; O. Ozturk; T. Yoshimura; T. Kawabata |
F. Teraoka; K. Fuji; O. Ozturk; T. Yoshimura; T. Kawabata |
F. Teraoka; K. Fuji; O. Ozturk; T. Yoshimura; T. Kawabata |
Asymmetric carbonyl migration of α-amino acid derivatives via memory of chirality |
Asymmetric carbonyl migration of α-amino acid derivatives via memory of chirality |
Asymmetric carbonyl migration of α-amino acid derivatives via memory of chirality |
Synlett, 2011, 4, 543-546 |
Synlett, 2011, 4, 543-546 |
Synlett, 2011, 4, 543-546 |
2011/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
2011/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Organocatalytic chemoselective monoacylation of 1,n-linear diols |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
Angewandte Chemie International Edition, 50, 21, 4888-4892 |
2011/05 |
Refereed |
English |
Research paper(scientific journal) |
Disclose to all |
T. Furuta; T. Kawabata |
T. Furuta; T. Kawabata |
T. Furuta; T. Kawabata |
最新のトピック 触媒的位置選択的官能基化 -次世代の分子変換法 |
最新のトピック 触媒的位置選択的官能基化 -次世代の分子変換法 |
最新のトピック 触媒的位置選択的官能基化 -次世代の分子変換法 |
化学, 2011, 66, 70-71 |
化学, 2011, 66, 70-71 |
化学, 2011, 66, 70-71 |
2011 |
Refereed |
English |
Thesis(Others) |
Disclose to all |
J.B. Brown; T. Urata; T. Tamura; M.A. Arai; T. Kawabata; T. Akutsu |
J.B. Brown; T. Urata; T. Tamura; M.A. Arai; T. Kawabata; T. Akutsu |
J.B. Brown; T. Urata; T. Tamura; M.A. Arai; T. Kawabata; T. Akutsu |
Compound analysis via graph kernels incorporating chirality  |
Compound analysis via graph kernels incorporating chirality  |
Compound analysis via graph kernels incorporating chirality  |
Journal of Bioinformatics and Computational Biology, 8, 63-81 |
Journal of Bioinformatics and Computational Biology, 8, 63-81 |
Journal of Bioinformatics and Computational Biology, 8, 63-81 |
2010/12 |
Refereed |
English |
|
Disclose to all |
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
2010/10/15 |
Refereed |
English |
|
Disclose to all |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
K. Yoshida; T. Furuta; T. Kawabata |
Perfectly regioselective acylation of a cardiac glycoside, digitoxin, via catalytic amplification of the intrinsic reactivity  |
Perfectly regioselective acylation of a cardiac glycoside, digitoxin, via catalytic amplification of the intrinsic reactivity  |
Perfectly regioselective acylation of a cardiac glycoside, digitoxin, via catalytic amplification of the intrinsic reactivity  |
Tetrahedron Letters, 51, 37, 4830-4832 |
Tetrahedron Letters, 51, 37, 4830-4832 |
Tetrahedron Letters, 51, 37, 4830-4832 |
2010/09/15 |
Refereed |
English |
|
Disclose to all |
K. Hayashi; N. Matubayasi; C. Jiang; T. Yoshimura; S. Majumdar; T. Sasamori; N. Tokitoh; T. Kawabata |
K. Hayashi; N. Matubayasi; C. Jiang; T. Yoshimura; S. Majumdar; T. Sasamori; N. Tokitoh; T. Kawabata |
K. Hayashi; N. Matubayasi; C. Jiang; T. Yoshimura; S. Majumdar; T. Sasamori; N. Tokitoh; T. Kawabata |
Insights into the origins of configurational stability of axially chiral biaryl amines with an intramolecular N-H-N hydrogen bond |
Insights into the origins of configurational stability of axially chiral biaryl amines with an intramolecular N-H-N hydrogen bond |
Insights into the origins of configurational stability of axially chiral biaryl amines with an intramolecular N-H-N hydrogen bond |
Journal of Organic Chemistry, 75, 15, 5031-5036 |
Journal of Organic Chemistry, 75, 15, 5031-5036 |
Journal of Organic Chemistry, 75, 15, 5031-5036 |
2010/08/06 |
Refereed |
English |
|
Disclose to all |
K. Hayashi; Y. Nakajima; F. Ozawa; T. Kawabata |
K. Hayashi; Y. Nakajima; F. Ozawa; T. Kawabata |
K. Hayashi; Y. Nakajima; F. Ozawa; T. Kawabata |
Axially chiral anilido-aldimine aluminum complexes with a pseudobinaphthyl skeleton  |
Axially chiral anilido-aldimine aluminum complexes with a pseudobinaphthyl skeleton  |
Axially chiral anilido-aldimine aluminum complexes with a pseudobinaphthyl skeleton  |
Chemistry Letters, 39, 6, 643-645 |
Chemistry Letters, 39, 6, 643-645 |
Chemistry Letters, 39, 6, 643-645 |
2010/06/05 |
Refereed |
English |
|
Disclose to all |
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
Perfectly regioselective and sequential protection of glucopyranosides |
Perfectly regioselective and sequential protection of glucopyranosides |
Perfectly regioselective and sequential protection of glucopyranosides |
European Journal of Organic Chemistry, 5, 827-831 |
European Journal of Organic Chemistry, 5, 827-831 |
European Journal of Organic Chemistry, 5, 827-831 |
2010/02 |
Refereed |
English |
|
Disclose to all |
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
Organic Letters, 12, 2, 256-258 |
Organic Letters, 12, 2, 256-258 |
Organic Letters, 12, 2, 256-258 |
2010/01/15 |
Refereed |
English |
|
Disclose to all |
Y. Ueda; W. Muramatsu; K. Mishiro; T. Furuta; T. Kawabata |
Y. Ueda; W. Muramatsu; K. Mishiro; T. Furuta; T. Kawabata |
Y. Ueda; W. Muramatsu; K. Mishiro; T. Furuta; T. Kawabata |
Functional group tolerance in organocatalytic regioselective acylation of carbohydrates |
Functional group tolerance in organocatalytic regioselective acylation of carbohydrates |
Functional group tolerance in organocatalytic regioselective acylation of carbohydrates |
Journal of Organic Chemistry, 74, 22, 8802-8805 |
Journal of Organic Chemistry, 74, 22, 8802-8805 |
Journal of Organic Chemistry, 74, 22, 8802-8805 |
2009/11/20 |
Refereed |
English |
|
Disclose to all |
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
Synthesis and properties of S,R-alternating octinaphthalenes |
Synthesis and properties of S,R-alternating octinaphthalenes |
Synthesis and properties of S,R-alternating octinaphthalenes |
Tetrahedron, 65, 31, 6135-6140 |
Tetrahedron, 65, 31, 6135-6140 |
Tetrahedron, 65, 31, 6135-6140 |
2009/08/01 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; T. Furuta |
T. Kawabata; T. Furuta |
T. Kawabata; T. Furuta |
Nonenzymatic regioselective acylation of carbohydrates |
Nonenzymatic regioselective acylation of carbohydrates |
Nonenzymatic regioselective acylation of carbohydrates |
Chemistry Letters, 38, 7, 640-647 |
Chemistry Letters, 38, 7, 640-647 |
Chemistry Letters, 38, 7, 640-647 |
2009/07/05 |
Refereed |
English |
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Disclose to all |
D. Sue; K. Takaishi; T. Harada; R. Kuroda; T. Kawabata; K. Tsubaki |
D. Sue; K. Takaishi; T. Harada; R. Kuroda; T. Kawabata; K. Tsubaki |
D. Sue; K. Takaishi; T. Harada; R. Kuroda; T. Kawabata; K. Tsubaki |
Synthesis of chiral dotriacontanaphthalenes: How many naphthalene units are we able to elaborately connect? |
Synthesis of chiral dotriacontanaphthalenes: How many naphthalene units are we able to elaborately connect? |
Synthesis of chiral dotriacontanaphthalenes: How many naphthalene units are we able to elaborately connect? |
Journal of Organic Chemistry, 74, 10, 3940-3943 |
Journal of Organic Chemistry, 74, 10, 3940-3943 |
Journal of Organic Chemistry, 74, 10, 3940-3943 |
2009/05/15 |
Refereed |
English |
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Disclose to all |
T. Kawabata; C. Jiang; K. Hayashi; K. Tsubaki; T. Yoshimura; S. Majumdar; T. Sasamori; N. Tokitoh |
T. Kawabata; C. Jiang; K. Hayashi; K. Tsubaki; T. Yoshimura; S. Majumdar; T. Sasamori; N. Tokitoh |
T. Kawabata; C. Jiang; K. Hayashi; K. Tsubaki; T. Yoshimura; S. Majumdar; T. Sasamori; N. Tokitoh |
Axially chiral binaphthyl surrogates with an inner N-H-N hydrogen bond |
Axially chiral binaphthyl surrogates with an inner N-H-N hydrogen bond |
Axially chiral binaphthyl surrogates with an inner N-H-N hydrogen bond |
Journal of the American Chemical Society, 131, 1, 54-55 |
Journal of the American Chemical Society, 131, 1, 54-55 |
Journal of the American Chemical Society, 131, 1, 54-55 |
2009 |
Refereed |
English |
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Disclose to all |
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
2009 |
Refereed |
English |
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Disclose to all |
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
2009 |
Refereed |
English |
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Disclose to all |
川端猛夫 |
川端猛夫 |
|
単糖類の4位選択的アシル化触媒 |
単糖類の4位選択的アシル化触媒 |
|
和光純薬時報, 76, 4, 16-19 |
和光純薬時報, 76, 4, 16-19 |
, 76, 4, 16-19 |
2008/10/24 |
|
Japanese |
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Disclose to all |
T. Kawabata; K. Moriyama; S. Kawakami; K. Tsubaki |
T. Kawabata; K. Moriyama; S. Kawakami; K. Tsubaki |
T. Kawabata; K. Moriyama; S. Kawakami; K. Tsubaki |
Powdered KOH in OMSO: An efficient base for asymmetric cyclization via memory of chirality at ambient temperature |
Powdered KOH in OMSO: An efficient base for asymmetric cyclization via memory of chirality at ambient temperature |
Powdered KOH in OMSO: An efficient base for asymmetric cyclization via memory of chirality at ambient temperature |
Journal of the American Chemical Society, 130, 12, 4153-4157 |
Journal of the American Chemical Society, 130, 12, 4153-4157 |
Journal of the American Chemical Society, 130, 12, 4153-4157 |
2008/03/26 |
Refereed |
English |
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Disclose to all |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
Synthesis, 28, 5, 747-753 |
Synthesis, 28, 5, 747-753 |
Synthesis, 28, 5, 747-753 |
2008/03/03 |
Refereed |
English |
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Disclose to all |
Tsubaki K, Takaishi K, Sue D, Matsuda K, Kanemitsu Y, Kawabata T |
Tsubaki K, Takaishi K, Sue D, Matsuda K, Kanemitsu Y, Kawabata T |
Tsubaki K, Takaishi K, Sue D, Matsuda K, Kanemitsu Y, Kawabata T |
Thress-Component Cascade Energy Transfer Using Oligonaphthalene Skeletons |
Thress-Component Cascade Energy Transfer Using Oligonaphthalene Skeletons |
Thress-Component Cascade Energy Transfer Using Oligonaphthalene Skeletons |
J. Org. Chem., 73, 4279-4282 |
J. Org. Chem., 73, 4279-4282 |
J. Org. Chem., 73, 4279-4282 |
2008 |
Refereed |
English |
|
Disclose to all |
T. Watanabe; T. Kawabata |
T. Watanabe; T. Kawabata |
T. Watanabe; T. Kawabata |
Asymmetric dieckmann condensation via memory of chirality: synthesis of the key intermediate for as-3201, an aldose reductase inhibitor |
Asymmetric dieckmann condensation via memory of chirality: synthesis of the key intermediate for as-3201, an aldose reductase inhibitor |
Asymmetric dieckmann condensation via memory of chirality: synthesis of the key intermediate for as-3201, an aldose reductase inhibitor |
Heterocycles, 76, 2, 1593-1606 |
Heterocycles, 76, 2, 1593-1606 |
Heterocycles, 76, 2, 1593-1606 |
2008 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; K. Takaishi; D. Sue; K. Matsuda; Y. Kanemitsu; T. Kawabata |
K. Tsubaki; K. Takaishi; D. Sue; K. Matsuda; Y. Kanemitsu; T. Kawabata |
K. Tsubaki; K. Takaishi; D. Sue; K. Matsuda; Y. Kanemitsu; T. Kawabata |
Three-component cascade energy transfer with use of oligonaphthalene skeletons |
Three-component cascade energy transfer with use of oligonaphthalene skeletons |
Three-component cascade energy transfer with use of oligonaphthalene skeletons |
Journal of Organic Chemistry, 73, 11, 4279-4282 |
Journal of Organic Chemistry, 73, 11, 4279-4282 |
Journal of Organic Chemistry, 73, 11, 4279-4282 |
2008 |
Refereed |
English |
|
Disclose to all |
K. Moriyama; H. Sakai; T. Kawabata |
K. Moriyama; H. Sakai; T. Kawabata |
K. Moriyama; H. Sakai; T. Kawabata |
Direct asymmetric intramolecular alkylation of β-alkoxy-α-amino esters via memory of chirality |
Direct asymmetric intramolecular alkylation of β-alkoxy-α-amino esters via memory of chirality |
Direct asymmetric intramolecular alkylation of β-alkoxy-α-amino esters via memory of chirality |
Organic Letters, 10, 17, 3883-3886 |
Organic Letters, 10, 17, 3883-3886 |
Organic Letters, 10, 17, 3883-3886 |
2008 |
Refereed |
English |
|
Disclose to all |
T. Kawabata |
T. Kawabata |
T. Kawabata |
An organocatalytic regioselective acylation of carbohydrates: Toward the development of intelligent catalysts |
An organocatalytic regioselective acylation of carbohydrates: Toward the development of intelligent catalysts |
An organocatalytic regioselective acylation of carbohydrates: Toward the development of intelligent catalysts |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 65, 11, 1081-1088 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 65, 11, 1081-1088 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 65, 11, 1081-1088 |
2007/11 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
2007/10/24 |
Refereed |
English |
|
Disclose to all |
W. Muramatsu; T. Kawabata |
W. Muramatsu; T. Kawabata |
W. Muramatsu; T. Kawabata |
Regioselective acylation of 6-O-protected octyl β-d-glucopyranosides by DMAP catalysis |
Regioselective acylation of 6-O-protected octyl β-d-glucopyranosides by DMAP catalysis |
Regioselective acylation of 6-O-protected octyl β-d-glucopyranosides by DMAP catalysis |
Tetrahedron Letters, 48, 29, 5031-5033 |
Tetrahedron Letters, 48, 29, 5031-5033 |
Tetrahedron Letters, 48, 29, 5031-5033 |
2007/07/16 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
2007/05/25 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
2007/05/16 |
Refereed |
English |
|
Disclose to all |
川端 猛夫 |
川端 猛夫 |
|
魅力的な分子変換へのアプローチ |
魅力的な分子変換へのアプローチ |
|
ファルマシア, 43, 3, 242-244 |
ファルマシア, 43, 3, 242-244 |
, 43, 3, 242-244 |
2007/03/01 |
Refereed |
Japanese |
|
Disclose to all |
K. Tsubaki; D. Tanima; T. Sasamori; N. Tokitoh; T. Kawabata |
K. Tsubaki; D. Tanima; T. Sasamori; N. Tokitoh; T. Kawabata |
K. Tsubaki; D. Tanima; T. Sasamori; N. Tokitoh; T. Kawabata |
Colorimetric recognition of the length of α,ω-diamines in water |
Colorimetric recognition of the length of α,ω-diamines in water |
Colorimetric recognition of the length of α,ω-diamines in water |
Tetrahedron Letters, 48, 12, 2135-2138 |
Tetrahedron Letters, 48, 12, 2135-2138 |
Tetrahedron Letters, 48, 12, 2135-2138 |
2007 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
Bidirectional and colorimetric recognition of sodium and potassium ions |
Bidirectional and colorimetric recognition of sodium and potassium ions |
Bidirectional and colorimetric recognition of sodium and potassium ions |
Organic Letters, 8, 25, 5797-5800 |
Organic Letters, 8, 25, 5797-5800 |
Organic Letters, 8, 25, 5797-5800 |
2006/12/07 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S. Matsuda; S. Kawakami; D. Monguchi; K. Moriyama |
T. Kawabata; S. Matsuda; S. Kawakami; D. Monguchi; K. Moriyama |
T. Kawabata; S. Matsuda; S. Kawakami; D. Monguchi; K. Moriyama |
Stereochemical diversity in asymmetric cyclization via memory of chirality |
Stereochemical diversity in asymmetric cyclization via memory of chirality |
Stereochemical diversity in asymmetric cyclization via memory of chirality |
Journal of the American Chemical Society, 128, 48, 15394-15395 |
Journal of the American Chemical Society, 128, 48, 15394-15395 |
Journal of the American Chemical Society, 128, 48, 15394-15395 |
2006/12/06 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; M. Sakakibara; Y. Nakatani; T. Kawabata |
K. Tsubaki; M. Sakakibara; Y. Nakatani; T. Kawabata |
K. Tsubaki; M. Sakakibara; Y. Nakatani; T. Kawabata |
Suzuki-Miyaura coupling on the three upper rims of hexahomotrioxacalix[3]arenes |
Suzuki-Miyaura coupling on the three upper rims of hexahomotrioxacalix[3]arenes |
Suzuki-Miyaura coupling on the three upper rims of hexahomotrioxacalix[3]arenes |
Tetrahedron, 62, 44, 10321-10324 |
Tetrahedron, 62, 44, 10321-10324 |
Tetrahedron, 62, 44, 10321-10324 |
2006/10/29 |
Refereed |
English |
|
Disclose to all |
K. Takaishi; K. Tsubaki; H. Tanaka; M. Miura; T. Kawabata |
K. Takaishi; K. Tsubaki; H. Tanaka; M. Miura; T. Kawabata |
K. Takaishi; K. Tsubaki; H. Tanaka; M. Miura; T. Kawabata |
Synthesis and optical properties of the helical oligonaphthalenes |
Synthesis and optical properties of the helical oligonaphthalenes |
Synthesis and optical properties of the helical oligonaphthalenes |
Yakugaku Zasshi, 126, 9, 779-787 |
Yakugaku Zasshi, 126, 9, 779-787 |
Yakugaku Zasshi, 126, 9, 779-787 |
2006/09 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; H. Tanaka; K. Takaishi; M. Miura; H. Morikawa; T. Furuta; K. Tanaka; K. Fuji; T. Sasamori; N. Tokitoh; T. Kawabata |
K. Tsubaki; H. Tanaka; K. Takaishi; M. Miura; H. Morikawa; T. Furuta; K. Tanaka; K. Fuji; T. Sasamori; N. Tokitoh; T. Kawabata |
K. Tsubaki; H. Tanaka; K. Takaishi; M. Miura; H. Morikawa; T. Furuta; K. Tanaka; K. Fuji; T. Sasamori; N. Tokitoh; T. Kawabata |
Bottom-up synthesis of optically active oligonaphthalenes: Three different pathways for controlling axial chirality |
Bottom-up synthesis of optically active oligonaphthalenes: Three different pathways for controlling axial chirality |
Bottom-up synthesis of optically active oligonaphthalenes: Three different pathways for controlling axial chirality |
Journal of Organic Chemistry, 71, 17, 6579-6587 |
Journal of Organic Chemistry, 71, 17, 6579-6587 |
Journal of Organic Chemistry, 71, 17, 6579-6587 |
2006/08/18 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; K. Takaishi; H. Tanaka; M. Miura; T. Kawabata |
K. Tsubaki; K. Takaishi; H. Tanaka; M. Miura; T. Kawabata |
K. Tsubaki; K. Takaishi; H. Tanaka; M. Miura; T. Kawabata |
Long-range exciton-coupled circular dichroism: Application for determination of the absolute configuration of oligonaphthalenes |
Long-range exciton-coupled circular dichroism: Application for determination of the absolute configuration of oligonaphthalenes |
Long-range exciton-coupled circular dichroism: Application for determination of the absolute configuration of oligonaphthalenes |
Organic Letters, 8, 12, 2587-2590 |
Organic Letters, 8, 12, 2587-2590 |
Organic Letters, 8, 12, 2587-2590 |
2006/06/08 |
Refereed |
English |
|
Disclose to all |
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
Tetrahedron, 62, 8, 1756-1763 |
Tetrahedron, 62, 8, 1756-1763 |
Tetrahedron, 62, 8, 1756-1763 |
2006/02/20 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
Tetrahedron Letters, 47, 8, 1241-1244 |
Tetrahedron Letters, 47, 8, 1241-1244 |
Tetrahedron Letters, 47, 8, 1241-1244 |
2006/02/20 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
2005/06/10 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; T. Kusumoto; N. Hayashi; D. Tanima; K. Fuji; T. Kawabata |
K. Tsubaki; T. Kusumoto; N. Hayashi; D. Tanima; K. Fuji; T. Kawabata |
K. Tsubaki; T. Kusumoto; N. Hayashi; D. Tanima; K. Fuji; T. Kawabata |
Convenient preparation of optically active N,N-bis(4-substituted-4- aminobutyl)amines |
Convenient preparation of optically active N,N-bis(4-substituted-4- aminobutyl)amines |
Convenient preparation of optically active N,N-bis(4-substituted-4- aminobutyl)amines |
Tetrahedron Asymmetry, 16, 3, 739-743 |
Tetrahedron Asymmetry, 16, 3, 739-743 |
Tetrahedron Asymmetry, 16, 3, 739-743 |
2005/02/07 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; J. Chen; H. Suzuki; K. Fuji |
T. Kawabata; J. Chen; H. Suzuki; K. Fuji |
T. Kawabata; J. Chen; H. Suzuki; K. Fuji |
Stereochemical study on α-alkylation of β-branched α-amino acid derivatives via memory of chirality |
Stereochemical study on α-alkylation of β-branched α-amino acid derivatives via memory of chirality |
Stereochemical study on α-alkylation of β-branched α-amino acid derivatives via memory of chirality |
Synthesis, 8, 1368-1377 |
Synthesis, 8, 1368-1377 |
Synthesis, 8, 1368-1377 |
2005 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
2005 |
Refereed |
English |
|
Disclose to all |
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
2004/11/12 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; M. Miura; H. Morikawa; H. Tanaka; T. Kawabata; T. Furuta; K. Tanaka; K. Fuji |
K. Tsubaki; M. Miura; H. Morikawa; H. Tanaka; T. Kawabata; T. Furuta; K. Tanaka; K. Fuji |
K. Tsubaki; M. Miura; H. Morikawa; H. Tanaka; T. Kawabata; T. Furuta; K. Tanaka; K. Fuji |
Synthesis of Optically Active Oligonaphthalenes via Second-Order Asymmetric Transformation |
Synthesis of Optically Active Oligonaphthalenes via Second-Order Asymmetric Transformation |
Synthesis of Optically Active Oligonaphthalenes via Second-Order Asymmetric Transformation |
Journal of the American Chemical Society, 125, 52, 16200-16201 |
Journal of the American Chemical Society, 125, 52, 16200-16201 |
Journal of the American Chemical Society, 125, 52, 16200-16201 |
2003/12/31 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S. Kawakami; S. Majumdar |
T. Kawabata; S. Kawakami; S. Majumdar |
T. Kawabata; S. Kawakami; S. Majumdar |
Asymmetric Cyclization via Memory of Chirality: A Concise Access to Cyclic Amino Acids with a Quaternary Stereocenter |
Asymmetric Cyclization via Memory of Chirality: A Concise Access to Cyclic Amino Acids with a Quaternary Stereocenter |
Asymmetric Cyclization via Memory of Chirality: A Concise Access to Cyclic Amino Acids with a Quaternary Stereocenter |
Journal of the American Chemical Society, 125, 43, 13012-13013 |
Journal of the American Chemical Society, 125, 43, 13012-13013 |
Journal of the American Chemical Society, 125, 43, 13012-13013 |
2003/10/29 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
Tetrahedron Letters, 44, 8, 1545-1548 |
Tetrahedron Letters, 44, 8, 1545-1548 |
Tetrahedron Letters, 44, 8, 1545-1548 |
2003/02/17 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S.-P. Kawakami; S. Shimada; K. Fuji |
T. Kawabata; S. P. Kawakami; S. Shimada; K. Fuji |
T. Kawabata; S.-P. Kawakami; S. Shimada; K. Fuji |
Control of the enantioselectivity of alkylation of phenylalanine derivatives by regulation of the aggregate structure of chiral enolate intermediates |
Control of the enantioselectivity of alkylation of phenylalanine derivatives by regulation of the aggregate structure of chiral enolate intermediates |
Control of the enantioselectivity of alkylation of phenylalanine derivatives by regulation of the aggregate structure of chiral enolate intermediates |
Tetrahedron, 59, 7, 965-974 |
Tetrahedron, 59, 7, 965-974 |
Tetrahedron, 59, 7, 965-974 |
2003/02/10 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; R. Stragies; T. Fukaya; K. Fuji |
T. Kawabata; R. Stragies; T. Fukaya; K. Fuji |
T. Kawabata; R. Stragies; T. Fukaya; K. Fuji |
Remote chirality transfer in nucleophilic catalysis with N-(4-pyridinyl)-L-proline derivatives |
Remote chirality transfer in nucleophilic catalysis with N-(4-pyridinyl)-L-proline derivatives |
Remote chirality transfer in nucleophilic catalysis with N-(4-pyridinyl)-L-proline derivatives |
Chirality, 15, 1, 71-76 |
Chirality, 15, 1, 71-76 |
Chirality, 15, 1, 71-76 |
2003/01 |
Refereed |
English |
|
Disclose to all |
T. Kawabata |
T. Kawabata |
T. Kawabata |
Asymmetric Construction of Quaternary Carbon Centers. |
Asymmetric Construction of Quaternary Carbon Centers. |
Asymmetric Construction of Quaternary Carbon Centers. |
Farumashia, 39, 114-115 |
Farumashia, 39, 114-115 |
Farumashia, 39, 114-115 |
2003 |
Refereed |
English |
|
Disclose to all |
Kawabata, T; Fuji, K |
T. Kawabata; K. Fuji |
Kawabata, T; Fuji, K |
Memory of chirality: Asymmetric induction based on the dynamic chirality of enolates |
Memory of chirality: Asymmetric induction based on the dynamic chirality of enolates |
Memory of chirality: Asymmetric induction based on the dynamic chirality of enolates |
TOPICS IN STEREOCHEMISTRY, VOL 23, 23, 175-205 |
TOPICS IN STEREOCHEMISTRY, VOL 23, 23, 175-205 |
TOPICS IN STEREOCHEMISTRY, VOL 23, 23, 175-205 |
2003 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; O. Öztürk; J. Chen; K. Fuji |
T. Kawabata; O. ?zt?rk; J. Chen; K. Fuji |
T. Kawabata; O. Öztürk; J. Chen; K. Fuji |
Chirality transfer during alkylation of chiral amides |
Chirality transfer during alkylation of chiral amides |
Chirality transfer during alkylation of chiral amides |
Chemical Communications, 1, 162-163 |
Chemical Communications, 1, 162-163 |
Chemical Communications, 1, 162-163 |
2003 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S.-P. Kawakami; K. Fuji |
T. Kawabata; S.-P. Kawakami; K. Fuji |
T. Kawabata; S.-P. Kawakami; K. Fuji |
Enantioselective α-allylation of a phenylalanine derivative under the control of aggregation of a chiral nonracemic enolate |
Enantioselective α-allylation of a phenylalanine derivative under the control of aggregation of a chiral nonracemic enolate |
Enantioselective α-allylation of a phenylalanine derivative under the control of aggregation of a chiral nonracemic enolate |
Tetrahedron Letters, 43, 8, 1465-1467 |
Tetrahedron Letters, 43, 8, 1465-1467 |
Tetrahedron Letters, 43, 8, 1465-1467 |
2002/02/18 |
Refereed |
English |
|
Disclose to all |
T.D. Bagul; G. Lakshmaiah; T. Kawabata; K. Fuji |
T.D. Bagul; G. Lakshmaiah; T. Kawabata; K. Fuji |
T.D. Bagul; G. Lakshmaiah; T. Kawabata; K. Fuji |
Total synthesis of spirotryprostatin B via asymmetric nitroolefination |
Total synthesis of spirotryprostatin B via asymmetric nitroolefination |
Total synthesis of spirotryprostatin B via asymmetric nitroolefination |
Organic Letters, 4, 2, 249-251 |
Organic Letters, 4, 2, 249-251 |
Organic Letters, 4, 2, 249-251 |
2002/01/24 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; K. Yamamoto; Y. Momose; H. Yoshida; Y. Nagaoka; K. Fuji |
T. Kawabata; K. Yamamoto; Y. Momose; H. Yoshida; Y. Nagaoka; K. Fuji |
T. Kawabata; K. Yamamoto; Y. Momose; H. Yoshida; Y. Nagaoka; K. Fuji |
Kinetic resolution of amino alcohol derivatives with a chiral nucleophilic catalyst: Access to enantiopure cyclic cis-amino alcohols |
Kinetic resolution of amino alcohol derivatives with a chiral nucleophilic catalyst: Access to enantiopure cyclic cis-amino alcohols |
Kinetic resolution of amino alcohol derivatives with a chiral nucleophilic catalyst: Access to enantiopure cyclic cis-amino alcohols |
Chemical Communications, 24, 2700-2701 |
Chemical Communications, 24, 2700-2701 |
Chemical Communications, 24, 2700-2701 |
2001/12/21 |
Refereed |
English |
|
Disclose to all |
T. Kawabata |
T. Kawabata |
T. Kawabata |
Discrimination of Enantiomers by an Artificial Enzyme. |
Discrimination of Enantiomers by an Artificial Enzyme. |
Discrimination of Enantiomers by an Artificial Enzyme. |
Bio Industry, 18, 17-24 |
Bio Industry, 18, 17-24 |
Bio Industry, 18, 17-24 |
2001 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
Organic Letters, 2, 24, 3883-3885 |
Organic Letters, 2, 24, 3883-3885 |
Organic Letters, 2, 24, 3883-3885 |
2000/11/30 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; H. Suzuki; Y. Nagae; K. Fuji |
T. Kawabata; H. Suzuki; Y. Nagae; K. Fuji |
T. Kawabata; H. Suzuki; Y. Nagae; K. Fuji |
A chiral nonracemic enolate with dynamic axial chirality: Direct asymmetric α-methylation of α-amino acid derivatives |
A chiral nonracemic enolate with dynamic axial chirality: Direct asymmetric α-methylation of α-amino acid derivatives |
A chiral nonracemic enolate with dynamic axial chirality: Direct asymmetric α-methylation of α-amino acid derivatives |
Angewandte Chemie - International Edition, 39, 12, 2155-2157 |
Angewandte Chemie - International Edition, 39, 12, 2155-2157 |
Angewandte Chemie - International Edition, 39, 12, 2155-2157 |
2000 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; K. Fuji |
T. Kawabata; K. Fuji |
T. Kawabata; K. Fuji |
Memory of chirality: Alkylation of α-amino acid derivatives |
Memory of chirality: Alkylation of α-amino acid derivatives |
Memory of chirality: Alkylation of α-amino acid derivatives |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 58, 11, 1095-1099 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 58, 11, 1095-1099 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 58, 11, 1095-1099 |
2000 |
Refereed |
English |
|
Disclose to all |
T. Kawabata |
T. Kawabata |
T. Kawabata |
Asymmetric synthesis based on enolate chemistry: β-lactam synthesis and memory of chirality |
Asymmetric synthesis based on enolate chemistry: β-lactam synthesis and memory of chirality |
Asymmetric synthesis based on enolate chemistry: β-lactam synthesis and memory of chirality |
Reviews on Heteroatom Chemistry, 22, 33-58 |
Reviews on Heteroatom Chemistry, 22, 33-58 |
Reviews on Heteroatom Chemistry, 22, 33-58 |
2000 |
Refereed |
English |
|
Disclose to all |
G. Lakshmaiah; T. Kawabata; M. Shang; K. Fuji |
G. Lakshmaiah; T. Kawabata; M. Shang; K. Fuji |
G. Lakshmaiah; T. Kawabata; M. Shang; K. Fuji |
Total synthesis of (-)-horsfiline via asymmetric nitroolefination |
Total synthesis of (-)-horsfiline via asymmetric nitroolefination |
Total synthesis of (-)-horsfiline via asymmetric nitroolefination |
Journal of Organic Chemistry, 64, 5, 1699-1704 |
Journal of Organic Chemistry, 64, 5, 1699-1704 |
Journal of Organic Chemistry, 64, 5, 1699-1704 |
1999/03/05 |
Refereed |
English |
|
Disclose to all |
K. Fuji; N. Kinoshita; K. Tanaka; T. Kawabata |
K. Fuji; N. Kinoshita; K. Tanaka; T. Kawabata |
K. Fuji; N. Kinoshita; K. Tanaka; T. Kawabata |
Enantioselective allylic substitution catalyzed by an iridium complex: Remarkable effects of the counter cation |
Enantioselective allylic substitution catalyzed by an iridium complex: Remarkable effects of the counter cation |
Enantioselective allylic substitution catalyzed by an iridium complex: Remarkable effects of the counter cation |
Chemical Communications, 22, 2289-2290 |
Chemical Communications, 22, 2289-2290 |
Chemical Communications, 22, 2289-2290 |
1999 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
Tetrahedron Letters, 39, 35, 6323-6326 |
Tetrahedron Letters, 39, 35, 6323-6326 |
Tetrahedron Letters, 39, 35, 6323-6326 |
1998/08/27 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Oka; T. Kawabata; T. Kinoshita |
K. Fuji; T. Oka; T. Kawabata; T. Kinoshita |
K. Fuji; T. Oka; T. Kawabata; T. Kinoshita |
The first synthesis of an optically active molecular bevel gear with only two cogs on each wheel |
The first synthesis of an optically active molecular bevel gear with only two cogs on each wheel |
The first synthesis of an optically active molecular bevel gear with only two cogs on each wheel |
Tetrahedron Letters, 39, 11, 1373-1376 |
Tetrahedron Letters, 39, 11, 1373-1376 |
Tetrahedron Letters, 39, 11, 1373-1376 |
1998/03/12 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata |
K. Fuji; T. Kawabata |
K. Fuji; T. Kawabata |
Memory of chirality - A new principle in enolate chemistry |
Memory of chirality - A new principle in enolate chemistry |
Memory of chirality - A new principle in enolate chemistry |
Chemistry - A European Journal, 4, 3, 373-376 |
Chemistry - A European Journal, 4, 3, 373-376 |
Chemistry - A European Journal, 4, 3, 373-376 |
1998/03 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; T. Ohmori; M. Shang; M. Node |
K. Fuji; T. Kawabata; T. Ohmori; M. Shang; M. Node |
K. Fuji; T. Kawabata; T. Ohmori; M. Shang; M. Node |
Enantioselective creation of quaternary carbon centers through addition-elimination reaction: Asymmetric nitroolefination of 3-substituted 2-oxindoles |
Enantioselective creation of quaternary carbon centers through addition-elimination reaction: Asymmetric nitroolefination of 3-substituted 2-oxindoles |
Enantioselective creation of quaternary carbon centers through addition-elimination reaction: Asymmetric nitroolefination of 3-substituted 2-oxindoles |
Heterocycles, 47, 2, 951-964 |
Heterocycles, 47, 2, 951-964 |
Heterocycles, 47, 2, 951-964 |
1998/02/01 |
Refereed |
English |
|
Disclose to all |
T. Kawabate; M. Nagato; K. Takasu; K. Fuji |
T. Kawabate; M. Nagato; K. Takasu; K. Fuji |
T. Kawabate; M. Nagato; K. Takasu; K. Fuji |
Nonenzymatic kinetic resolution of racemic alcohols through an \\'induced fit\\' process |
Nonenzymatic kinetic resolution of racemic alcohols through an \\'induced fit\\' process |
Nonenzymatic kinetic resolution of racemic alcohols through an \\'induced fit\\' process |
Journal of the American Chemical Society, 119, 13, 3169-3170 |
Journal of the American Chemical Society, 119, 13, 3169-3170 |
Journal of the American Chemical Society, 119, 13, 3169-3170 |
1997/04/02 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Sakurai; N. Tohkai; A. Kuroda; T. Kawabata; Y. Fukazawa; T. Kinoshita; T. Tada |
K. Fuji; M. Sakurai; N. Tohkai; A. Kuroda; T. Kawabata; Y. Fukazawa; T. Kinoshita; T. Tada |
K. Fuji; M. Sakurai; N. Tohkai; A. Kuroda; T. Kawabata; Y. Fukazawa; T. Kinoshita; T. Tada |
Unexpectedly facile racemization of 8-diphenylphosphinoyl-8′-methoxy-1,1′-binaphthyl |
Unexpectedly facile racemization of 8-diphenylphosphinoyl-8′-methoxy-1,1′-binaphthyl |
Unexpectedly facile racemization of 8-diphenylphosphinoyl-8′-methoxy-1,1′-binaphthyl |
Chemical Communications, 14, 1609-1610 |
Chemical Communications, 14, 1609-1610 |
Chemical Communications, 14, 1609-1610 |
1996/07/21 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; A. Kuroda; E. Nakata; K. Takasu; K. Fuji |
T. Kawabata; A. Kuroda; E. Nakata; K. Takasu; K. Fuji |
T. Kawabata; A. Kuroda; E. Nakata; K. Takasu; K. Fuji |
Chiral recognition of amino acid derivatives by 1,1′-binaphthalene-8,8′-diol |
Chiral recognition of amino acid derivatives by 1,1′-binaphthalene-8,8′-diol |
Chiral recognition of amino acid derivatives by 1,1′-binaphthalene-8,8′-diol |
Tetrahedron Letters, 37, 24, 4153-4156 |
Tetrahedron Letters, 37, 24, 4153-4156 |
Tetrahedron Letters, 37, 24, 4153-4156 |
1996/06/10 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; Y. Kiryu; Y. Sugiura |
K. Fuji; T. Kawabata; Y. Kiryu; Y. Sugiura |
K. Fuji; T. Kawabata; Y. Kiryu; Y. Sugiura |
Ring opening of optically active cis-disubstituted aziridino alcohols: An enantiodivergent synthesis of functionalized amino alcohol derivatives |
Ring opening of optically active cis-disubstituted aziridino alcohols: An enantiodivergent synthesis of functionalized amino alcohol derivatives |
Ring opening of optically active cis-disubstituted aziridino alcohols: An enantiodivergent synthesis of functionalized amino alcohol derivatives |
Heterocycles, 42, 2, 701-722 |
Heterocycles, 42, 2, 701-722 |
Heterocycles, 42, 2, 701-722 |
1996/01/01 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
1995/04/07 |
Refereed |
English |
|
Disclose to all |
FUJI, K; KAWABATA, T; OHMORI, T; NODE, M |
K. Fuji; T. Kawabata; T. Ohmori; M. Node |
FUJI, K; KAWABATA, T; OHMORI, T; NODE, M |
AN ENANTIOSELECTIVE SYNTHESIS OF (-)-PSEUDOPHRYNAMINOL THROUGH ASYMMETRIC NITROOLEFINATION |
AN ENANTIOSELECTIVE SYNTHESIS OF (-)-PSEUDOPHRYNAMINOL THROUGH ASYMMETRIC NITROOLEFINATION |
AN ENANTIOSELECTIVE SYNTHESIS OF (-)-PSEUDOPHRYNAMINOL THROUGH ASYMMETRIC NITROOLEFINATION |
SYNLETT, 4, 367-368 |
SYNLETT, 4, 367-368 |
SYNLETT, 4, 367-368 |
1995/04 |
Refereed |
English |
|
Disclose to all |
T. Kawabata |
T. Kawabata |
T. Kawabata |
Memory of Chirality: An Idea Realizing Unusual Organic Reactions. |
Memory of Chirality: An Idea Realizing Unusual Organic Reactions. |
Memory of Chirality: An Idea Realizing Unusual Organic Reactions. |
Chemistry Today, 287, 16-21 |
Chemistry Today, 287, 16-21 |
Chemistry Today, 287, 16-21 |
1995 |
Refereed |
English |
|
Disclose to all |
T. Kawabata, K. Fuji |
T. Kawabata, K. Fuji |
T. Kawabata, K. Fuji |
Memory of Chirality: A New Concept for Enolate Chemistry. |
Memory of Chirality: A New Concept for Enolate Chemistry. |
Memory of Chirality: A New Concept for Enolate Chemistry. |
Cemistry and Chemical Industry (Japan), 48, 1039-1042 |
Cemistry and Chemical Industry (Japan), 48, 1039-1042 |
Cemistry and Chemical Industry (Japan), 48, 1039-1042 |
1995 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; T. Wirth; K. Yahiro; H. Suzuki; K. Fuji |
T. Kawabata; T. Wirth; K. Yahiro; H. Suzuki; K. Fuji |
T. Kawabata; T. Wirth; K. Yahiro; H. Suzuki; K. Fuji |
Direct asymmetric α-alkylation of phenylalanine derivatives using no external chiral sources |
Direct asymmetric α-alkylation of phenylalanine derivatives using no external chiral sources |
Direct asymmetric α-alkylation of phenylalanine derivatives using no external chiral sources |
Journal of the American Chemical Society, 116, 23, 10809-10810 |
Journal of the American Chemical Society, 116, 23, 10809-10810 |
Journal of the American Chemical Society, 116, 23, 10809-10810 |
1994/11/16 |
Refereed |
English |
|
Disclose to all |
Takeo Kawabata; Kaoru Fuji |
Takeo Kawabata; Kaoru Fuji |
Takeo Kawabata; Kaoru Fuji |
Memory of chirality |
Memory of chirality |
Memory of chirality |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 52, 7, 589-595 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 52, 7, 589-595 |
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 52, 7, 589-595 |
1994/07 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
Tetrahedron Letters, 34, 32, 5127-5130 |
Tetrahedron Letters, 34, 32, 5127-5130 |
Tetrahedron Letters, 34, 32, 5127-5130 |
1993/08/06 |
Refereed |
English |
|
Disclose to all |
T. Kawabata, K. Fuji |
T. Kawabata, K. Fuji |
T. Kawabata, K. Fuji |
Asymmetric Carbon-Carbon Bond Formation. |
Asymmetric Carbon-Carbon Bond Formation. |
Asymmetric Carbon-Carbon Bond Formation. |
Chemistry and Biology, 31, 817-825 |
Chemistry and Biology, 31, 817-825 |
Chemistry and Biology, 31, 817-825 |
1993 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; T. Minami; T. Hiyama |
T. Kawabata; T. Minami; T. Hiyama |
T. Kawabata; T. Minami; T. Hiyama |
Stereoselective synthesis of β-lactams by oxidative coupling of dianions of acyclic tertiary amides |
Stereoselective synthesis of β-lactams by oxidative coupling of dianions of acyclic tertiary amides |
Stereoselective synthesis of β-lactams by oxidative coupling of dianions of acyclic tertiary amides |
Journal of Organic Chemistry, 57, 6, 1864-1873 |
Journal of Organic Chemistry, 57, 6, 1864-1873 |
Journal of Organic Chemistry, 57, 6, 1864-1873 |
1992/03/13 |
Refereed |
English |
|
Disclose to all |
KAWABATA, T; YAHIRO, K; FUJI, K |
T. Kawabata; K. Yahiro; K. Fuji |
KAWABATA, T; YAHIRO, K; FUJI, K |
MEMORY OF CHIRALITY - ENANTIOSELECTIVE ALKYLATION REACTIONS AT AN ASYMMETRIC CARBON ADJACENT TO A CARBONYL GROUP |
MEMORY OF CHIRALITY - ENANTIOSELECTIVE ALKYLATION REACTIONS AT AN ASYMMETRIC CARBON ADJACENT TO A CARBONYL GROUP |
MEMORY OF CHIRALITY - ENANTIOSELECTIVE ALKYLATION REACTIONS AT AN ASYMMETRIC CARBON ADJACENT TO A CARBONYL GROUP |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 113, 25, 9694-9696 |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 113, 25, 9694-9696 |
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 113, 25, 9694-9696 |
1991/12/04 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; Y. Kiryu; Y. Sugiura; T. Taga; Y. Miwa |
K. Fuji; T. Kawabata; Y. Kiryu; Y. Sugiura; T. Taga; Y. Miwa |
K. Fuji; T. Kawabata; Y. Kiryu; Y. Sugiura; T. Taga; Y. Miwa |
A new access to chiral aziridines by enzymatic transesterification of meso-bis(acetoxymethyl)aziridines |
A new access to chiral aziridines by enzymatic transesterification of meso-bis(acetoxymethyl)aziridines |
A new access to chiral aziridines by enzymatic transesterification of meso-bis(acetoxymethyl)aziridines |
Tetrahedron Letters, 31, 46, 6663-6666 |
Tetrahedron Letters, 31, 46, 6663-6666 |
Tetrahedron Letters, 31, 46, 6663-6666 |
1990 |
Refereed |
English |
|
Disclose to all |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
Tetrahedron, 46, 21, 7393-7402 |
Tetrahedron, 46, 21, 7393-7402 |
Tetrahedron, 46, 21, 7393-7402 |
1990 |
Refereed |
English |
|
Disclose to all |
FUJI, K; NODE, M; NANIWA, Y; KAWABATA, T |
K. Fuji; M. Node; Y. Naniwa; T. Kawabata |
FUJI, K; NODE, M; NANIWA, Y; KAWABATA, T |
ENANTIOSELECTIVE IODOLACTONIZATION THROUGH DIASTEREOTOPIC GROUP DIFFERENTIATION |
ENANTIOSELECTIVE IODOLACTONIZATION THROUGH DIASTEREOTOPIC GROUP DIFFERENTIATION |
ENANTIOSELECTIVE IODOLACTONIZATION THROUGH DIASTEREOTOPIC GROUP DIFFERENTIATION |
TETRAHEDRON LETTERS, 31, 22, 3175-3178 |
TETRAHEDRON LETTERS, 31, 22, 3175-3178 |
TETRAHEDRON LETTERS, 31, 22, 3175-3178 |
1990 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; K. Sumi; T. Hiyama |
T. Kawabata; K. Sumi; T. Hiyama |
T. Kawabata; K. Sumi; T. Hiyama |
A new synthesis of β-lactams through stereoselective oxidative coupling of the dianions of acyclic amides |
A new synthesis of β-lactams through stereoselective oxidative coupling of the dianions of acyclic amides |
A new synthesis of β-lactams through stereoselective oxidative coupling of the dianions of acyclic amides |
Journal of the American Chemical Society, 111, 17, 6843-6845 |
Journal of the American Chemical Society, 111, 17, 6843-6845 |
Journal of the American Chemical Society, 111, 17, 6843-6845 |
1989/08/16 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; K. Itoh; T. Hiyama |
T. Kawabata; K. Itoh; T. Hiyama |
T. Kawabata; K. Itoh; T. Hiyama |
Regio- and chemoselective epimerization of cis-3-amino-β-lactams to the trans-isomers: a new synthesis of aztreonam |
Regio- and chemoselective epimerization of cis-3-amino-β-lactams to the trans-isomers: a new synthesis of aztreonam |
Regio- and chemoselective epimerization of cis-3-amino-β-lactams to the trans-isomers: a new synthesis of aztreonam |
Tetrahedron Letters, 30, 36, 4837-4840 |
Tetrahedron Letters, 30, 36, 4837-4840 |
Tetrahedron Letters, 30, 36, 4837-4840 |
1989 |
Refereed |
English |
|
Disclose to all |
Y. Ito; Y. Kobayashi; T. Kawabata; M. Takase; S. Terashima |
Y. Ito; Y. Kobayashi; T. Kawabata; M. Takase; S. Terashima |
Y. Ito; Y. Kobayashi; T. Kawabata; M. Takase; S. Terashima |
Novel syntheses of the carbapenem key intermediates, (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone and (3S,4R)-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-4-carboxymethyl-2-azetidinone, from (S)-ethyl lactate |
Novel syntheses of the carbapenem key intermediates, (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone and (3S,4R)-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-4-carboxymethyl-2-azetidinone, from (S)-ethyl lactate |
Novel syntheses of the carbapenem key intermediates, (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone and (3S,4R)-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-4-carboxymethyl-2-azetidinone, from (S)-ethyl lactate |
Tetrahedron, 45, 18, 5767-5790 |
Tetrahedron, 45, 18, 5767-5790 |
Tetrahedron, 45, 18, 5767-5790 |
1989 |
Refereed |
English |
|
Disclose to all |
N. Takahashi; H. Osada; N. Numao; H. Saimoto; T. Kawabata; T. Hiyama |
N. Takahashi; H. Osada; N. Numao; H. Saimoto; T. Kawabata; T. Hiyama |
N. Takahashi; H. Osada; N. Numao; H. Saimoto; T. Kawabata; T. Hiyama |
Differentiation induction of human promyelocytic leukemia cells with colletochlorin B and its analogues |
Differentiation induction of human promyelocytic leukemia cells with colletochlorin B and its analogues |
Differentiation induction of human promyelocytic leukemia cells with colletochlorin B and its analogues |
Chemical and Pharmaceutical Bulletin, 36, 1, 452-455 |
Chemical and Pharmaceutical Bulletin, 36, 1, 452-455 |
Chemical and Pharmaceutical Bulletin, 36, 1, 452-455 |
1988 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; Y. Kimura; Y. Ito; S. Terashima; A. Sasaki; M. Sunagawa |
T. Kawabata; Y. Kimura; Y. Ito; S. Terashima; A. Sasaki; M. Sunagawa |
T. Kawabata; Y. Kimura; Y. Ito; S. Terashima; A. Sasaki; M. Sunagawa |
A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics employing [ 2+2 ]-cycloaddition reaction of diketene with a chiral imine |
A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics employing [ 2+2 ]-cycloaddition reaction of diketene with a chiral imine |
A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics employing [ 2+2 ]-cycloaddition reaction of diketene with a chiral imine |
Tetrahedron, 44, 8, 2149-2165 |
Tetrahedron, 44, 8, 2149-2165 |
Tetrahedron, 44, 8, 2149-2165 |
1988 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; P.A. Grieco; H.-L. Sham; H. Kim; J.Y. Jaw; S. Tu |
T. Kawabata; P.A. Grieco; H.-L. Sham; H. Kim; J.Y. Jaw; S. Tu |
T. Kawabata; P.A. Grieco; H.-L. Sham; H. Kim; J.Y. Jaw; S. Tu |
Model studies in the quassimarin series: Total synthesis of de-A-quassimarin |
Model studies in the quassimarin series: Total synthesis of de-A-quassimarin |
Model studies in the quassimarin series: Total synthesis of de-A-quassimarin |
Journal of Organic Chemistry, 52, 15, 3346-3354 |
Journal of Organic Chemistry, 52, 15, 3346-3354 |
Journal of Organic Chemistry, 52, 15, 3346-3354 |
1987/07/24 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
Journal of the Chemical Society, Perkin Transactions 1, 70, 5, 1043-1047 |
Journal of the Chemical Society, Perkin Transactions 1, 70, 5, 1043-1047 |
Journal of the Chemical Society, Perkin Transactions 1, 70, 5, 1043-1047 |
1987/05 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; Y. Kimura; Y. Ito; S. Terashima; A. Sasaki; M. Sunagawa |
T. Kawabata; Y. Kimura; Y. Ito; S. Terashima; A. Sasaki; M. Sunagawa |
T. Kawabata; Y. Kimura; Y. Ito; S. Terashima; A. Sasaki; M. Sunagawa |
A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics from (s)-methyl 3-hydroxy-2-methylpropionate |
A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics from (s)-methyl 3-hydroxy-2-methylpropionate |
A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics from (s)-methyl 3-hydroxy-2-methylpropionate |
Tetrahedron Letters, 27, 51, 6241-6244 |
Tetrahedron Letters, 27, 51, 6241-6244 |
Tetrahedron Letters, 27, 51, 6241-6244 |
1986 |
Refereed |
English |
|
Disclose to all |
Y. Ito; T. Kawabata; S. Terashima |
Y. Ito; T. Kawabata; S. Terashima |
Y. Ito; T. Kawabata; S. Terashima |
A novel synthesis of (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone, the versatile key intermediate of carbapenem synthesis, from (S)-ethyl lactate |
A novel synthesis of (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone, the versatile key intermediate of carbapenem synthesis, from (S)-ethyl lactate |
A novel synthesis of (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone, the versatile key intermediate of carbapenem synthesis, from (S)-ethyl lactate |
Tetrahedron Letters, 27, 47, 5751-5754 |
Tetrahedron Letters, 27, 47, 5751-5754 |
Tetrahedron Letters, 27, 47, 5751-5754 |
1986 |
Refereed |
English |
|
Disclose to all |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
Tetrahedron Letters, 26, 6, 779-782 |
Tetrahedron Letters, 26, 6, 779-782 |
Tetrahedron Letters, 26, 6, 779-782 |
1985/08 |
Refereed |
English |
|
Disclose to all |
M. Node; T. Kawabata; K. Ohta; M. Fujimoto; E. Fujita; K. Fuji |
M. Node; T. Kawabata; K. Ohta; M. Fujimoto; E. Fujita; K. Fuji |
M. Node; T. Kawabata; K. Ohta; M. Fujimoto; E. Fujita; K. Fuji |
Hard acid and soft nucleophile systems. 8. Reductive dehalogenation of o- and p-halophenols and their derivatives |
Hard acid and soft nucleophile systems. 8. Reductive dehalogenation of o- and p-halophenols and their derivatives |
Hard acid and soft nucleophile systems. 8. Reductive dehalogenation of o- and p-halophenols and their derivatives |
Journal of Organic Chemistry, 49, 19, 3641-3643 |
Journal of Organic Chemistry, 49, 19, 3641-3643 |
Journal of Organic Chemistry, 49, 19, 3641-3643 |
1984 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
Hard acid and soft nucleophile systems. 9. Cleavage of activated carbon-carbon double bonds with a hard Lewis acid and ethanethiol |
Hard acid and soft nucleophile systems. 9. Cleavage of activated carbon-carbon double bonds with a hard Lewis acid and ethanethiol |
Hard acid and soft nucleophile systems. 9. Cleavage of activated carbon-carbon double bonds with a hard Lewis acid and ethanethiol |
Journal of Organic Chemistry, 49, 17, 3214-3216 |
Journal of Organic Chemistry, 49, 17, 3214-3216 |
Journal of Organic Chemistry, 49, 17, 3214-3216 |
1984 |
Refereed |
English |
|
Disclose to all |
FUJI, K; NODE, M; KAWABATA, T; FUJIMOTO, M |
K. Fuji; M. Node; T. Kawabata; FUJIMOTO, M |
FUJI, K; NODE, M; KAWABATA, T; FUJIMOTO, M |
HARD-SOFT AFFINITY INVERSION - DEHALOGENATION OF ALPHA-HALOKETONES |
HARD-SOFT AFFINITY INVERSION - DEHALOGENATION OF ALPHA-HALOKETONES |
HARD-SOFT AFFINITY INVERSION - DEHALOGENATION OF ALPHA-HALOKETONES |
CHEMISTRY LETTERS, 7, 1153-1156 |
CHEMISTRY LETTERS, 7, 1153-1156 |
CHEMISTRY LETTERS, 7, 1153-1156 |
1984 |
Refereed |
English |
|
Disclose to all |
NODE, M; KAWABATA, T; FUJIMOTO, M; FUJI, K |
M. Node; T. Kawabata; M. Fujimoto; K. Fuji; |
NODE, M; KAWABATA, T; FUJIMOTO, M; FUJI, K |
GENERAL-SYNTHESIS OF 1-ETHYLTHIO-2-NITROOLEFINS |
GENERAL-SYNTHESIS OF 1-ETHYLTHIO-2-NITROOLEFINS |
GENERAL-SYNTHESIS OF 1-ETHYLTHIO-2-NITROOLEFINS |
SYNTHESIS-STUTTGART, 3, 234-236 |
SYNTHESIS-STUTTGART, 3, 234-236 |
SYNTHESIS-STUTTGART, 3, 234-236 |
1984 |
Refereed |
English |
|
Disclose to all |
M. Node; T. Kawabata; M. Ueda; M. Fujimoto; K. Fuji; E. Fujita |
M. Node; T. Kawabata; M. Ueda; M. Fujimoto; K. Fuji; E. Fujita |
M. Node; T. Kawabata; M. Ueda; M. Fujimoto; K. Fuji; E. Fujita |
Reductive displacement of the nitro group into hydrogen in primary α-nitroketones |
Reductive displacement of the nitro group into hydrogen in primary α-nitroketones |
Reductive displacement of the nitro group into hydrogen in primary α-nitroketones |
Tetrahedron Letters, 23, 39, 4047-4050 |
Tetrahedron Letters, 23, 39, 4047-4050 |
Tetrahedron Letters, 23, 39, 4047-4050 |
1982 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
Carbon-carbon double bond cleavage with a hard lewis acid and ethanethiol |
Carbon-carbon double bond cleavage with a hard lewis acid and ethanethiol |
Carbon-carbon double bond cleavage with a hard lewis acid and ethanethiol |
Tetrahedron Letters, 22, 9, 875-878 |
Tetrahedron Letters, 22, 9, 875-878 |
Tetrahedron Letters, 22, 9, 875-878 |
1981 |
Refereed |
English |
|
Disclose to all |
Kawabata T, Fuji K |
T. Kawabata; K. Fuji |
Kawabata T, Fuji K |
Carbon-Carbon Bond Formation |
Carbon-Carbon Bond Formation |
Carbon-Carbon Bond Formation |
Asymmetric Synthesis, Kodansha, Tokyo, , 184, 216, 285, 337 |
Asymmetric Synthesis, Kodansha, Tokyo, , 184, 216, 285, 337 |
Asymmetric Synthesis, Kodansha, Tokyo, , 184, 216, 285, 337 |
|
Refereed |
English |
|
Disclose to all |
T. Kawabata |
T. Kawabata |
T. Kawabata |
Nucleophilic Catalysis: Asymmetric Synthesis, Substrate-Specific Reactions and Multi-Component Sequential Reactions. |
Nucleophilic Catalysis: Asymmetric Synthesis, Substrate-Specific Reactions and Multi-Component Sequential Reactions. |
Nucleophilic Catalysis: Asymmetric Synthesis, Substrate-Specific Reactions and Multi-Component Sequential Reactions. |
J. Syn.Org. Chem. Jpn., , 458-459 |
J. Syn.Org. Chem. Jpn., , 458-459 |
J. Syn.Org. Chem. Jpn., , 458-459 |
|
Refereed |
English |
|
Disclose to all |
T. Kawabata, K. Fuji |
T. Kawabata, K. Fuji |
T. Kawabata, K. Fuji |
Memory of Chirality: Asymmetric C-C Bond Formation via Enolate Intermediates with Dynamic Chirality. |
Memory of Chirality: Asymmetric C-C Bond Formation via Enolate Intermediates with Dynamic Chirality. |
Memory of Chirality: Asymmetric C-C Bond Formation via Enolate Intermediates with Dynamic Chirality. |
J. Syn. Org. Chem. Jpn., , 66-67 |
J. Syn. Org. Chem. Jpn., , 66-67 |
J. Syn. Org. Chem. Jpn., , 66-67 |
|
Refereed |
English |
|
Disclose to all |
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
|
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
|
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
, 75, 20, 7010-7013 |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
2010/10/15 |
Refereed |
English |
|
Disclose to all |
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
|
T. Furuta; J. Yamamoto; Y. Kitamura; A. Hashimoto; H. Masu; I. Azumaya; T. Kan; T. Kawabata |
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
|
Synthesis of axially chiral amino acid and amino alcohols via additive-ligand-free Pd-catalyzed domino coupling reaction and subsequent transformations of the product amidoaza[5]helicene |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
, 75, 20, 7010-7013 |
Journal of Organic Chemistry, 75, 20, 7010-7013 |
2010/10/15 |
Refereed |
English |
|
Disclose to all |
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
|
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
Perfectly regioselective and sequential protection of glucopyranosides |
|
Perfectly regioselective and sequential protection of glucopyranosides |
European Journal of Organic Chemistry, 5, 827-831 |
, 5, 827-831 |
European Journal of Organic Chemistry, 5, 827-831 |
2010/02 |
Refereed |
English |
|
Disclose to all |
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
|
W. Muramatsu; K. Mishiro; Y. Ueda; T. Furuta; T. Kawabata |
Perfectly regioselective and sequential protection of glucopyranosides |
|
Perfectly regioselective and sequential protection of glucopyranosides |
European Journal of Organic Chemistry, 5, 827-831 |
, 5, 827-831 |
European Journal of Organic Chemistry, 5, 827-831 |
2010/02 |
Refereed |
English |
|
Disclose to all |
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
|
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
|
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
Organic Letters, 12, 2, 256-258 |
, 12, 2, 256-258 |
Organic Letters, 12, 2, 256-258 |
2010/01/15 |
Refereed |
English |
|
Disclose to all |
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
|
D. Sue; T. Kawabata; T. Sasamori; N. Tokitoh; K. Tsubaki |
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
|
Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction |
Organic Letters, 12, 2, 256-258 |
, 12, 2, 256-258 |
Organic Letters, 12, 2, 256-258 |
2010/01/15 |
Refereed |
English |
|
Disclose to all |
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
|
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
Synthesis and properties of S,R-alternating octinaphthalenes |
|
Synthesis and properties of S,R-alternating octinaphthalenes |
Tetrahedron, 65, 31, 6135-6140 |
, 65, 31, 6135-6140 |
Tetrahedron, 65, 31, 6135-6140 |
2009/08/01 |
Refereed |
English |
|
Disclose to all |
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
|
K. Takaishi; D. Sue; S. Kuwahara; N. Harada; T. Kawabata; K. Tsubaki |
Synthesis and properties of S,R-alternating octinaphthalenes |
|
Synthesis and properties of S,R-alternating octinaphthalenes |
Tetrahedron, 65, 31, 6135-6140 |
, 65, 31, 6135-6140 |
Tetrahedron, 65, 31, 6135-6140 |
2009/08/01 |
Refereed |
English |
|
Disclose to all |
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
|
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
|
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
, 48, 37, 6853-6856 |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
2009 |
Refereed |
English |
|
Disclose to all |
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
|
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
|
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
, 7, 22, 4689-4694 |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
2009 |
Refereed |
English |
|
Disclose to all |
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
|
Y. Azuma; M. Imanishi; T. Yoshimura; T. Kawabata; S. Futaki |
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
|
Cobalt(II)-responsive DNA binding of a GCN4-bZIP protein containing cysteine residues functionalized. with iminodiacetic acid |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
, 48, 37, 6853-6856 |
Angewandte Chemie - International Edition, 48, 37, 6853-6856 |
2009 |
Refereed |
English |
|
Disclose to all |
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
|
D. Tanima; Y. Imamura; T. Kawabata; K. Tsubaki |
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
|
Development of highly sensitive and selective molecules for detection of spermidine and spermine |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
, 7, 22, 4689-4694 |
Organic and Biomolecular Chemistry, 7, 22, 4689-4694 |
2009 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
|
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
|
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
Synthesis, 5, 747-753 |
, 5, 747-753 |
Synthesis, 5, 747-753 |
2008/03/03 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
|
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; Y. Uruno; R. Stragies |
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
|
Regioselective acylation of octyl β-D-glucopyranoside by chiral 4-pyrrolidinopyridine analogues |
Synthesis, 28, 5, 747-753 |
, 28, 5, 747-753 |
Synthesis, 28, 5, 747-753 |
2008/03/03 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
|
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
|
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
, 129, 42, 12890-12895 |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
2007/10/24 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
|
T. Kawabata; W. Muramatsu; T. Nishio; T. Shibata; H. Schedel |
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
|
A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
, 129, 42, 12890-12895 |
Journal of the American Chemical Society, 129, 42, 12890-12895 |
2007/10/24 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
|
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
|
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
, 72, 11, 4238-4241 |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
2007/05/25 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
|
K. Tsubaki; K. Takaishi; D. Sue; T. Kawabata |
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
|
Synthesis and determination of the absolute configuration of chiral tetracosanaphthalenes |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
, 72, 11, 4238-4241 |
Journal of Organic Chemistry, 72, 11, 4238-4241 |
2007/05/25 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
|
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
|
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
, 18, 8, 1017-1021 |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
2007/05/16 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
|
K. Tsubaki; D.T.T. Hai; V.K. Reddy; H. Ohnishi; K. Fuji; T. Kawabata |
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
|
Synthesis of chiral 2,2′-dimethyl-1,1′-binaphthyl-8,8′-diamine and barriers of atropisomerization of the related binaphthyls |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
, 18, 8, 1017-1021 |
Tetrahedron Asymmetry, 18, 8, 1017-1021 |
2007/05/16 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
|
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
Bidirectional and colorimetric recognition of sodium and potassium ions |
|
Bidirectional and colorimetric recognition of sodium and potassium ions |
Organic Letters, 8, 25, 5797-5800 |
, 8, 25, 5797-5800 |
Organic Letters, 8, 25, 5797-5800 |
2006/12/07 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
|
K. Tsubaki; D. Tanima; Y. Kuroda; K. Fuji; T. Kawabata |
Bidirectional and colorimetric recognition of sodium and potassium ions |
|
Bidirectional and colorimetric recognition of sodium and potassium ions |
Organic Letters, 8, 25, 5797-5800 |
, 8, 25, 5797-5800 |
Organic Letters, 8, 25, 5797-5800 |
2006/12/07 |
Refereed |
English |
|
Disclose to all |
D. Monguchi; S. Majumdar; T. Kawabata |
|
D. Monguchi; S. Majumdar; T. Kawabata |
Synthesis of chiral 1,2-dihydropyridines and 2,3,4-trisubstituted pyridines from α-amino acids |
|
Synthesis of chiral 1,2-dihydropyridines and 2,3,4-trisubstituted pyridines from α-amino acids |
Heterocycles, 68, 12, 2571-2578 |
, 68, 12, 2571-2578 |
Heterocycles, 68, 12, 2571-2578 |
2006/12/01 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
|
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
|
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
Tetrahedron Letters, 47, 8, 1241-1244 |
, 47, 8, 1241-1244 |
Tetrahedron Letters, 47, 8, 1241-1244 |
2006/02/20 |
Refereed |
English |
|
Disclose to all |
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
|
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
|
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
Tetrahedron, 62, 8, 1756-1763 |
, 62, 8, 1756-1763 |
Tetrahedron, 62, 8, 1756-1763 |
2006/02/20 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
|
K. Tsubaki; M. Miura; A. Nakamura; T. Kawabata |
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
|
Optical properties of oligo(2,3-dioxyfunctionalized)naphthalenes |
Tetrahedron Letters, 47, 8, 1241-1244 |
, 47, 8, 1241-1244 |
Tetrahedron Letters, 47, 8, 1241-1244 |
2006/02/20 |
Refereed |
English |
|
Disclose to all |
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
|
N. Kinoshita; T. Kawabata; K. Tsubaki; M. Bando; K. Fuji |
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
|
Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation |
Tetrahedron, 62, 8, 1756-1763 |
, 62, 8, 1756-1763 |
Tetrahedron, 62, 8, 1756-1763 |
2006/02/20 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
|
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
|
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
, 70, 12, 4609-4616 |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
2005/06/10 |
Refereed |
English |
|
Disclose to all |
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
|
K. Tsubaki; D. Tanima; M. Nuruzzaman; T. Kusumoto; K. Fuji; T. Kawabata |
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
|
Visual enantiomeric recognition of amino acid derivatives in protic solvents |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
, 70, 12, 4609-4616 |
Journal of Organic Chemistry, 70, 12, 4609-4616 |
2005/06/10 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
|
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
|
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
, 3, 9, 1609-1611 |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
2005 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
|
T. Kawabata; S. Majumdar; K. Tsubaki; D. Monguchi |
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
|
Memory of chirality in intramolecular conjugate addition of enolates: A novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
, 3, 9, 1609-1611 |
Organic and Biomolecular Chemistry, 3, 9, 1609-1611 |
2005 |
Refereed |
English |
|
Disclose to all |
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
|
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
|
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
, 69, 23, 7960-7964 |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
2004/11/12 |
Refereed |
English |
|
Disclose to all |
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
|
N. Kinoshita; K.H. Marx; K. Tanaka; K. Tsubaki; T. Kawabata; N. Yoshikai; E. Nakamura; K. Fuji |
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
|
Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
, 69, 23, 7960-7964 |
Journal of Organic Chemistry, 69, 23, 7960-7964 |
2004/11/12 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; O. Öztürk; H. Suzuki; K. Fuji |
|
T. Kawabata; O. Öztürk; H. Suzuki; K. Fuji |
A facile asymmetric synthesis of tetrahydroisoquinoline and tryptoline derivatives with a quaternary carbon center at C(3) |
|
A facile asymmetric synthesis of tetrahydroisoquinoline and tryptoline derivatives with a quaternary carbon center at C(3) |
Synthesis, 4, 505-508 |
, 4, 505-508 |
Synthesis, 4, 505-508 |
2003/03 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
|
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
|
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
Tetrahedron Letters, 44, 8, 1545-1548 |
, 44, 8, 1545-1548 |
Tetrahedron Letters, 44, 8, 1545-1548 |
2003/02/17 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
|
T. Kawabata; R. Stragies; T. Fukaya; Y. Nagaoka; H. Schedel; K. Fuji |
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
|
Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains |
Tetrahedron Letters, 44, 8, 1545-1548 |
, 44, 8, 1545-1548 |
Tetrahedron Letters, 44, 8, 1545-1548 |
2003/02/17 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
|
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
|
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
Organic Letters, 2, 24, 3883-3885 |
, 2, 24, 3883-3885 |
Organic Letters, 2, 24, 3883-3885 |
2000/11/30 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
|
T. Kawabata; J. Chen; H. Suzuki; Y. Nagae; T. Kinoshita; S. Chancharunee; K. Fuji |
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
|
Memory of Chirality in Diastereoselective α-alkylation of Isoleucine and allo-isoleucine Derivatives |
Organic Letters, 2, 24, 3883-3885 |
, 2, 24, 3883-3885 |
Organic Letters, 2, 24, 3883-3885 |
2000/11/30 |
Refereed |
English |
|
Disclose to all |
K. Fuji; H. Ohnishi; S. Moriyama; K. Tanaka; T. Kawabata; K. Tsubaki |
|
K. Fuji; H. Ohnishi; S. Moriyama; K. Tanaka; T. Kawabata; K. Tsubaki |
Palladium-catalyzed asymmetric allylic alkylation with a chiral monodentate phosphine ligand: 8-Diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
|
Palladium-catalyzed asymmetric allylic alkylation with a chiral monodentate phosphine ligand: 8-Diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
Synlett, 3, 351-352 |
, 3, 351-352 |
Synlett, 3, 351-352 |
2000/03 |
Refereed |
English |
|
Disclose to all |
J.-J. Chen; T. Kawabata; H. Ohnishi; M. Shang; K. Fuji |
|
J.-J. Chen; T. Kawabata; H. Ohnishi; M. Shang; K. Fuji |
Lewis acid-promoted nitroolefination of enol silyl ethers via an addition elimination process |
|
Lewis acid-promoted nitroolefination of enol silyl ethers via an addition elimination process |
Chemical and Pharmaceutical Bulletin, 47, 3, 394-397 |
, 47, 3, 394-397 |
Chemical and Pharmaceutical Bulletin, 47, 3, 394-397 |
1999/03 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
|
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
|
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
Tetrahedron Letters, 39, 35, 6323-6326 |
, 39, 35, 6323-6326 |
Tetrahedron Letters, 39, 35, 6323-6326 |
1998/08/27 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
|
K. Fuji; M. Sakurai; T. Kinoshita; T. Kawabata |
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
|
Palladium-catalyzed asymmetric reduction of allylic esters with a new chiral monodentate ligand, 8-diphenylphosphino-8\\'-methoxy-1,1\\'-binaphthyl |
Tetrahedron Letters, 39, 35, 6323-6326 |
, 39, 35, 6323-6326 |
Tetrahedron Letters, 39, 35, 6323-6326 |
1998/08/27 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Sakurai; T. Kinoshita; T. Tada; A. Kuroda; T. Kawabata |
|
K. Fuji; M. Sakurai; T. Kinoshita; T. Tada; A. Kuroda; T. Kawabata |
Assessment of the activity of 8\\'diphenylphosphino-8\\'-methoxy-1,1\\'- binaphthyl as a ligand for palladium-catalyzed reactions |
|
Assessment of the activity of 8\\'diphenylphosphino-8\\'-methoxy-1,1\\'- binaphthyl as a ligand for palladium-catalyzed reactions |
Chemical and Pharmaceutical Bulletin, 45, 9, 1524-1526 |
, 45, 9, 1524-1526 |
Chemical and Pharmaceutical Bulletin, 45, 9, 1524-1526 |
1997/09 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
|
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
|
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
, 60, 7, 1914-1915 |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
1995/04/07 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
|
K. Fuji; T. Kawabata; A. Kuroda; T. Taga |
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
|
Enantioselective protonation of enolates: Novel chiral proton sources and remarkable effects of the countercation |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
, 60, 7, 1914-1915 |
Journal of Organic Chemistry, 60, 7, 1914-1915 |
1995/04/07 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; Y. Naniwa; T. Ohmori; M. Node |
|
K. Fuji; T. Kawabata; Y. Naniwa; T. Ohmori; M. Node |
Enhanced reactivity of zinc enolates over lithium enolates in asymmetric nitroolefination |
|
Enhanced reactivity of zinc enolates over lithium enolates in asymmetric nitroolefination |
Chemical and Pharmaceutical Bulletin, 42, 4, 999-1001 |
, 42, 4, 999-1001 |
Chemical and Pharmaceutical Bulletin, 42, 4, 999-1001 |
1994/04 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
|
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
|
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
Tetrahedron Letters, 34, 32, 5127-5130 |
, 34, 32, 5127-5130 |
Tetrahedron Letters, 34, 32, 5127-5130 |
1993/08/06 |
Refereed |
English |
|
Disclose to all |
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
|
T. Kawabata; Y. Kiryu; Y. Sugiura; K. Fuji |
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
|
An enantiodivergent synthesis of threo β-amino alcohols: Preparation of key intermediates for bestatin and the related peptides |
Tetrahedron Letters, 34, 32, 5127-5130 |
, 34, 32, 5127-5130 |
Tetrahedron Letters, 34, 32, 5127-5130 |
1993/08/06 |
Refereed |
English |
|
Disclose to all |
M. Node; A. Itoh; K. Nishide; H. Abe; T. Kawabata; Y. Masaki; K. Fuji |
|
M. Node; A. Itoh; K. Nishide; H. Abe; T. Kawabata; Y. Masaki; K. Fuji |
Preparation of nitroalkenes: Substitution reaction via addition-elimination using β-nitrovinyl sulfoxides |
|
Preparation of nitroalkenes: Substitution reaction via addition-elimination using β-nitrovinyl sulfoxides |
Synthesis, 11, 1119-1124 |
, 11, 1119-1124 |
Synthesis, 11, 1119-1124 |
1992/11 |
Refereed |
English |
|
Disclose to all |
FUJI K;KAWABATA T;UEDA M;FUJIMOTO M;FUJITA E;NODE M |
|
FUJI K;KAWABATA T;UEDA M;FUJIMOTO M;FUJITA E;NODE M |
Hard Acid and Soft Nucleophile Systems. Part 14. On the Reactivity of .ALPHA.-Nitroketones and Nitroolefins Toward a Aluminum Chloride and Ethanethiol System. |
|
Hard Acid and Soft Nucleophile Systems. Part 14. On the Reactivity of .ALPHA.-Nitroketones and Nitroolefins Toward a Aluminum Chloride and Ethanethiol System. |
Bull Inst Chem Res Kyoto Univ, 70, 3, 318-325 |
, 70, 3, 318-325 |
Bull Inst Chem Res Kyoto Univ, 70, 3, 318-325 |
1992/10 |
Refereed |
English |
|
Disclose to all |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
|
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
|
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
Tetrahedron, 46, 21, 7393-7402 |
, 46, 21, 7393-7402 |
Tetrahedron, 46, 21, 7393-7402 |
1990 |
Refereed |
English |
|
Disclose to all |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
|
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. ltoh; Y. Masaki |
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
|
Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction |
Tetrahedron, 46, 21, 7393-7402 |
, 46, 21, 7393-7402 |
Tetrahedron, 46, 21, 7393-7402 |
1990 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
|
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
|
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
Journal of the Chemical Society, Perkin Transactions 1, 5, 1043-1047 |
, 5, 1043-1047 |
Journal of the Chemical Society, Perkin Transactions 1, 5, 1043-1047 |
1987/05 |
Refereed |
English |
|
Disclose to all |
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
|
K. Fuji; M. Node; T. Kawabata; M. Fujimoto |
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
|
Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: Dehalogenation of α-halogeno ketones with aluminium chloride and a thiol |
Journal of the Chemical Society, Perkin Transactions 1, 70, 5, 1043-1047 |
, 70, 5, 1043-1047 |
Journal of the Chemical Society, Perkin Transactions 1, 70, 5, 1043-1047 |
1987/05 |
Refereed |
English |
|
Disclose to all |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
|
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
|
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
Tetrahedron Letters, 26, 6, 779-782 |
, 26, 6, 779-782 |
Tetrahedron Letters, 26, 6, 779-782 |
1985/08 |
Refereed |
English |
|
Disclose to all |
NODE M;KAWABATA T;FUJITA E;FUJI K |
|
NODE M;KAWABATA T;FUJITA E;FUJI K |
Hard acid and soft nucleophile systems. 10. The mechanistic study for debromination of para-bromoanisole with aluminum chloride and ethanethiol. |
|
Hard acid and soft nucleophile systems. 10. The mechanistic study for debromination of para-bromoanisole with aluminum chloride and ethanethiol. |
Bull Inst Chem Res Kyoto Univ, 63, 2, 47-51 |
, 63, 2, 47-51 |
Bull Inst Chem Res Kyoto Univ, 63, 2, 47-51 |
1985/08 |
Refereed |
English |
|
Disclose to all |
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
|
K. Fuji; S.P. Khanapure; M. Node; T. Kawabata; A. Ito |
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
|
Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes |
Tetrahedron Letters, 26, 6, 779-782 |
, 26, 6, 779-782 |
Tetrahedron Letters, 26, 6, 779-782 |
1985 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
|
K. Fuji; T. Kawabata; M. Node; E. Fujita |
Hard acid and soft nucleophile systems. 9. Cleavage of activated carbon-carbon double bonds with a hard Lewis acid and ethanethiol |
|
Hard acid and soft nucleophile systems. 9. Cleavage of activated carbon-carbon double bonds with a hard Lewis acid and ethanethiol |
Journal of Organic Chemistry, 49, 17, 3214-3216 |
, 49, 17, 3214-3216 |
Journal of Organic Chemistry, 49, 17, 3214-3216 |
1984 |
Refereed |
English |
|
Disclose to all |
M. Node; T. Kawabata; K. Ohta; M. Fujimoto; E. Fujita; K. Fuji |
|
M. Node; T. Kawabata; K. Ohta; M. Fujimoto; E. Fujita; K. Fuji |
Hard acid and soft nucleophile systems. 8. Reductive dehalogenation of o- and p-halophenols and their derivatives |
|
Hard acid and soft nucleophile systems. 8. Reductive dehalogenation of o- and p-halophenols and their derivatives |
Journal of Organic Chemistry, 49, 19, 3641-3643 |
, 49, 19, 3641-3643 |
Journal of Organic Chemistry, 49, 19, 3641-3643 |
1984 |
Refereed |
English |
|
Disclose to all |
NODE, M; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
|
NODE, M; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
RADICAL CATION INDUCED REDUCTIVE DEHALOGENATION OF ORTHO-HALOPHENOLS AND PARA-HALOPHENOLS AND THEIR DERIVATIVES |
|
RADICAL CATION INDUCED REDUCTIVE DEHALOGENATION OF ORTHO-HALOPHENOLS AND PARA-HALOPHENOLS AND THEIR DERIVATIVES |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 2, 749-751 |
, 31, 2, 749-751 |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 2, 749-751 |
1983 |
Refereed |
English |
|
Disclose to all |
NODE, M; NISHIDE, K; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
|
NODE, M; NISHIDE, K; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
HARD ACID AND SOFT NUCLEOPHILE SYSTEM .7. A CONVENIENT REDUCTION OF FUNCTIONALIZED POLYARENES TO PARENT POLYARENES |
|
HARD ACID AND SOFT NUCLEOPHILE SYSTEM .7. A CONVENIENT REDUCTION OF FUNCTIONALIZED POLYARENES TO PARENT POLYARENES |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 12, 4306-4311 |
, 31, 12, 4306-4311 |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 12, 4306-4311 |
1983 |
Refereed |
English |
|
Disclose to all |
NODE, M; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
|
NODE, M; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
RADICAL CATION INDUCED REDUCTIVE DEHALOGENATION OF ORTHO-HALOPHENOLS AND PARA-HALOPHENOLS AND THEIR DERIVATIVES |
|
RADICAL CATION INDUCED REDUCTIVE DEHALOGENATION OF ORTHO-HALOPHENOLS AND PARA-HALOPHENOLS AND THEIR DERIVATIVES |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 2, 749-751 |
, 31, 2, 749-751 |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 2, 749-751 |
1983 |
Refereed |
English |
|
Disclose to all |
NODE, M; NISHIDE, K; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
|
NODE, M; NISHIDE, K; KAWABATA, T; OHTA, K; WATANABE, K; FUJI, K; FUJITA, E |
HARD ACID AND SOFT NUCLEOPHILE SYSTEM .7. A CONVENIENT REDUCTION OF FUNCTIONALIZED POLYARENES TO PARENT POLYARENES |
|
HARD ACID AND SOFT NUCLEOPHILE SYSTEM .7. A CONVENIENT REDUCTION OF FUNCTIONALIZED POLYARENES TO PARENT POLYARENES |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 12, 4306-4311 |
, 31, 12, 4306-4311 |
CHEMICAL & PHARMACEUTICAL BULLETIN, 31, 12, 4306-4311 |
1983 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; M. Node; E. Fujita |
|
K. Fuji; T. Kawabata; M. Node; E. Fujita |
Carbon-carbon double bond cleavage with a hard lewis acid and ethanethiol |
|
Carbon-carbon double bond cleavage with a hard lewis acid and ethanethiol |
Tetrahedron Letters, 22, 9, 875-878 |
, 22, 9, 875-878 |
Tetrahedron Letters, 22, 9, 875-878 |
1981 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; E. Fujita |
|
K. Fuji; T. Kawabata; E. Fujita |
Hard acid and soft nucleophile system. IV. Removal of benzyl protecting group with boron trifluoride etherate and dimethyl sulfide |
|
Hard acid and soft nucleophile system. IV. Removal of benzyl protecting group with boron trifluoride etherate and dimethyl sulfide |
Chemical and Pharmaceutical Bulletin, 28, 12, 3662-3664 |
, 28, 12, 3662-3664 |
Chemical and Pharmaceutical Bulletin, 28, 12, 3662-3664 |
1980 |
Refereed |
English |
|
Disclose to all |
K. Fuji; T. Kawabata; E. Fujita |
|
K. Fuji; T. Kawabata; E. Fujita |
Hard acid and soft nucleophile system. IV. Removal of benzyl protecting group with boron trifluoride etherate and dimethyl sulfide |
|
Hard acid and soft nucleophile system. IV. Removal of benzyl protecting group with boron trifluoride etherate and dimethyl sulfide |
Chemical and Pharmaceutical Bulletin, 28, 12, 3662-3664 |
, 28, 12, 3662-3664 |
Chemical and Pharmaceutical Bulletin, 28, 12, 3662-3664 |
1980 |
Refereed |
English |
|
Disclose to all |