Lipase-Catalyzed Transesterification of trans-2,5- Disubstituted Pyrrolidines : Effect of Substituent on Enantioselectivity
スポンサーリンク
概要
- 論文の詳細を見る
- 1998-12-05
著者
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KAWANAMI Yasuhiro
Department of Chemistry, Faculty of Education, Kagawa University
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Kawanami Y
Department Of Chemistry Faculty Of Education Kagawa University
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Kawanami Yasuhiro
Department Of Applied Biological Science Faculty Of Agriculture Kagawa University
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IIZUNA Noriko
Department of Chemistry, Faculty of Education, Kagawa University
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OKANO Kiyoka
Department of Chemistry, Faculty of Education, Kagawa University
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Iizuna Noriko
Department Of Chemistry Faculty Of Education Kagawa University
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Okano Kiyoka
Department Of Chemistry Faculty Of Education Kagawa University
関連論文
- Lipase-Catalyzed Kinetic Resolution of trans-2,5-Disubstituted Pyrrolidine Derivatives
- Retarding Activity of 6-O-Acyl-D-alloses against Plant Growth
- Practical Production of 6-O-Octanoyl-D-allose and Its Biological Activity on Plant Growth
- Synthesis of D-Allose Fatty Acid Esters via Lipase-Catalyzed Regioselective Transesterification
- 2-Geranyl-1,4-naphthoquinone, a Possible Intermediate of Anthraquinones in a Sesamum indicum Hairy Root Culture
- Highly Enantioselective Lipase-catalyzed Kinetic Resolution of 2-Silyloxy-1-propanol
- Lipase-Catalyzed Transesterification of trans-2,5- Disubstituted Pyrrolidines : Effect of Substituent on Enantioselectivity
- Enantioselective Reduction of Aliphatic Ketones Using Oxazaborolidine Catalyst Generated In Situ from Chiral Lactam Alcohol and Phenoxyborane
- Synthesis of thiol esters by carboxylic trichlorobenzoic anhydrides.
- Asymmetric Diels-Alder reaction of acrylamides having trans-2,5-disubstituted pyrrolidines as chiral auxiliaries.
- Diastereoselective reduction of .ALPHA.-keto amides having trans-2,5-disubstituted pyrrolidine as a chiral auxiliary.