松倉 弘子 | Riken Institute (The Institute of Physical and Chemical Research)
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概要
関連著者
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松倉 弘子
Riken Institute (The Institute of Physical and Chemical Research)
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大石 武
Riken Institute (The Institute of Physical and Chemical Research)
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松倉 弘子
Riken Institute(the Institute Of Physical And Chemical Research)
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大石 武
Faculty Of Engineering Yokohama National University:(present Address)meiji College Of Pharmacy
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大石 武
理研:(現)明治薬科大学
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秋田 弘幸
School Of Pharmaceutical Science Toho University
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秋田 弘幸
理化学研究所
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秋田 弘幸
School of Pharmaceutical Sciences, Toho University
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梅澤 勲
School of Pharmaceutical Science, Toho University
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梅澤 勲
School Of Pharmaceutical Science Toho University
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秋田 弘幸
Riken Institute (The Institute of Physical and Chemical Research)
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鷹野 道香
Riken Institute(the Insitute Of Physical And Chemical Research)
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梅澤 勲
Riken Institute (The Institute of Physical and Chemical Research)
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田中 渥夫
京大院・工・生化
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山田 治民
Riken Institute (the Institute Of Physical And Chemical Research)
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中田 忠
Riken Institute (The Institute of Physical and Chemical Research)
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松倉 弘子
理研
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園元 謙二
九工大・情報
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中田 忠
東京理大・理
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田中 渥夫
京大・工
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大山 智以子
Riken Institute(The Insitute of Physical and Chemical Research)
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TISNADJAJA Djadjat
Riken Institute(The Institute of Physical and Chemical Research)
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唐島 浩俊
Riken Institute (The Institute of Physical and Chemical Research)
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大石 武
(Present address)Meiji College of Pharmacy
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梅沢 勲
Riken Institute (The Institute of Physical and Chemical Research)
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園元 謙二
Laboratory of Industrial Biochemistry, Department of Industrial Chemistry, Faculty of Engineering, K
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田中 渥夫
Laboratory of Industrial Biochemistry, Department of Industrial Chemistry, Faculty of Engineering, K
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Tisnadjaja Djadjat
Riken Institute(the Institute Of Physical And Chemical Research):(present Address)indonesian Institu
著作論文
- The Regioselective Dehydration of Unsymmetrical Secondary Alcohols under Mitsunobu's Reaction Conditions
- A Facile Chemoenzymatic Route to Optically Active 4,5-Disubstituted-2E-hexenoate Derivatives. I
- Enantioselective Acetylation of an α-Hydroxy Ester by Using Ether-Linked Lipid-Lipase Aggregates in Organic Solvents
- A Formal Total Synthesis of (-)-Oudemansin B
- A Lipid-Lipase Aggregate with Ether Linkage as a New Type of Immobilized Enzyme for Enantioselective Hydrolysis in Organic Solvents
- A FACILE CHEMOENZYMATIC ROUTE TO ENANTIOMERICALLY PURE 4,5-DISUBSTITUTED-2-HEXENOATE DERIVATIVES
- A LIPID LIPASE AGGREGATE AS A NEW TYPE OF IMMOBILIZED ENZYME
- Asymmetric Reduction of α-Methyl β-Keto Esters by Microbial Cells Immobilized with Prepolymer(Organic,Chemical)
- SYNTHESIS OF USEFUL CHIRAL SYNTHONS (2R, 3R)-2-METHYLMALATE AND ITS CONGENERS VIA MICROBIAL ASYMMETRIC REDUCTION