Stereoselective coupling of optically active 3-trans-cinnamoyl-2-oxazolidinones with acid anhydrides by electroreduction

被引：15

作者：

Kise, N ^{[1
]}

Hirata, Y ^{[1
]}

Hamaguchi, T ^{[1
]}

Ueda, N ^{[1
]}

机构：

[1] Tottori Univ, Fac Engn, Dept Biotechnol, Tottori 6800945, Japan

来源：

TETRAHEDRON LETTERS | 1999年 / 40卷 / 46期

关键词：

acylation; coupling reaction; electrochemistry; lactones; oxazolidinones; reduction;

D O I：

10.1016/S0040-4039(99)01720-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The electronduction of chiral 3-trans-cinnamoyl-2-oxazolidinones with acid anhydrides gave beta-acylated products stereoselectively. The products were transformed to optically active cis-beta,gamma-disubstituted-gamma-lactones. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：8125 / 8128

页数：4

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