Chemoenzymatic Carbon-Carbon Bond Formation Leading to Non-carbohydrate Derivative. Stereoselective Synthesis of Pentamycin C-11-C-16 Fragment
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概要
- 論文の詳細を見る
Chemoenzymatic formation of 8 from an aldehyde 5 and dihydroxyacetone phosphate 6 was achieved by the use of fructose 1,6-diphosphate aldolase as a catalyst. Transformation of 8 to 20,corresponding to pentamycin C-11-C-16 fragment, was accomplished via 18a and 18b by chemical processes.
- 公益社団法人日本薬学会の論文
- 1993-02-15
著者
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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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大石 武
(Present address)Meiji College of Pharmacy
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嶋垣 正之
理研
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宗嶋 寛明
理研
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久保田 匡英
理研
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嶋垣 正之
The Institute of Physical and Chemical Research (RIKEN)
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宗嶋 寛明
The Institute of Physical and Chemical Research (RIKEN)
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久保田 匡英
The Institute of Physical and Chemical Research (RIKEN)
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