CHIRAL SYNTHESIS OF ENANTIO-TYPE ERYTHRINAN ALKALOIDS UTILIZING ASYMMETRIC ACYLATION AND KINETIC RESOLUTION OF DIASTEREOMERS
スポンサーリンク
概要
- 論文の詳細を見る
Chiral synthesis of an erythrinan alkaloid, (-)-3-demethoxyerythratidinone (11), as well as a versatile intermediate, the 1,7-cycloerythrinan derivative (14) (both are of enantio-type) was achieved using asymmetric acylation and kinetic resolution starting from the L-dopa derivative (1).
- 社団法人日本薬学会の論文
- 1992-11-25
著者
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津田 喜典
金沢大学
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津田 喜典
Faculty of Pharmaceutical Sciences, Kanazawa University
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細井 信造
Faculty of Pharmaceutical Sciences, Kanazawa University
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石田 和也
Faculty Of Pharmaceutical Sciences Kanazawa University
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三階 雅子
Faculty of Pharmaceutical Sciences, Kanazawa University
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細井 信造
金沢大薬
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津田 喜典
Faculty Of Pharmaceutical Sciences Kanazawa University
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三階 雅子
Faculty Of Pharmaceutical Sciences Kanazawa University
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