Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols

被引：14

作者：

Awale, S ^{[1
]}

Tezuka, Y ^{[1
]}

Wang, SM ^{[1
]}

Kadota, S ^{[1
]}

机构：

[1] Toyama Med & Pharmaceut Univ, Inst Nat Med, Sugitani, Toyama 9300194, Japan

来源：

ORGANIC LETTERS | 2002年 / 4卷 / 10期

关键词：

D O I：

10.1021/ol020042n

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[GRAPHICS] A highly efficient, facile, one-pot regioselective synthesis of a series of phenylpropanoid-substituted flavan-3-ols is described. The mechanism involves dienone-phenol rearrangement followed by a Michael-type reaction.

引用

页码：1707 / 1709

页数：3

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