Enantioselective synthesis of α-amino acids from nitroalkenes

被引：21

作者：

Sabelle, S

Lucet, D

Le Gall, T

Mioskowski, C

机构：

[1] CEA Saclay, Serv Mol Marquees, Dept Biol Cellulaire & Mol, F-91191 Gif Sur Yvette, France

[2] Univ Strasbourg 1, Fac Pharm, CNRS, Lab Synth Bioorgan, F-67401 Illkirch Graffenstaden, France

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 15期

关键词：

D O I：

10.1016/S0040-4039(98)00064-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The products of the conjugate addition of (R)-4-phenyl-2-oxazolidinone on monosubstituted nitroalkenes were converted into D-alpha-amino acids of high enantiomeric purity. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.

引用

页码：2111 / 2114

页数：4

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