Asymmetric Synthesis of (+)-and (-)-Batyl Alcohol, a Key Synthetic Intermediate for Platelet-Activating Factor, by Using Biocatalysts(Organic,Chemical)
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概要
- 論文の詳細を見る
Asymmetric synthesis of platelet-activating factor (PAF) and its enantiomer by using biocatalysts was studied. Microbial reduction of the pro-chiral α-ketoester (3) afforded (+)-4 (>99% ee), which could be converted to (+)- and (-)-batyl alcohol (12), a key synthetic intermediate for PAF. Compound (-)-4 (96% ee), with the requisite configuration for the synthesis of natural PAF, could also be obtained by enzyme-catalyzed enantioselective hydrolysis or (±)-15.
- 公益社団法人日本薬学会の論文
- 1987-08-25
著者
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酒井 浄
Faculty Of Pharmaceutical Sciences Kyushu University
-
Oishi T
Riken Inst. The Inst. Physical And Chemical Research Saitama Jpn
-
Akita H
Inst. Physical And Chemical Research
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Akita Hiroyuki
Riken Institute
-
Oishi Takeshi
Riken Institute (the Institute Of Physical And Chemical Research) Synthetic Organic Chemistry Labora
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SUEMUNE HIROSHI
Faculty of Pharmaceutical Sciences, Kyushu Uinversity
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MIZUHARA YUKAKO
Faculty of Pharmaceutical Sciences, Kyushu University
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AKITA HIROYUKI
The Institute of Physical and Chemical Research (Riken)
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OISHI TAKESHI
The Institute of Physical and Chemical Research (Riken)
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SAKI KIYOSHI
Faculty of Pharmaceutical Sciences, Kyushu University
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Suemune Hiroshi
Faculty Of Pharmaceutical Sciences Kyushu Uinversity
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Mizuhara Y
Kyushu Univ. Fukuoka Jpn
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OISHI Takeshi
The Institute of Physical and Chemical Research
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