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
收藏
页码：2111 / 2114
页数：4
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