EFFICIENT SYNTHESIS OF NATURAL (+)-COLLINUSIN USING CATALYTIC ASYMMETRIC HYDROGENATION WITH A CHIRAL BISPHOSPHINE-RHODIUM(I) COMPLEX

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概要

• 論文の詳細を見る

• (+)-Collinusin, a natural lignan lactone, has been synthesized by using the asymmetric hydrogenation of a α-veratrylidenesuccinic acid half ester with a (S, S)-MOD-DIOP-rhodium(I) complex catalyst as a key reaction, and the absolute configuration of the C-3 has been determined to be R__-.

• 公益社団法人日本薬学会の論文
• 1989-11-25

著者

• 阿知波 一雄

  School of Pharmaceutical Sciences, University of Shizuoka

• 森本 俊明

  School Of Pharmaceutical Sciences University

• 千葉 三男

  School Of Pharmaceutical Sciences University Of Shizuoka

• 千葉 三男

  Reserch Center, Toyotama Perfumery Co. Ltd.,

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