Metal halide-mediated opening of three membered rings: Enantioselective synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid and (3R)-3-aminodecanoic acid

被引：43

作者：

Righi, G ^{[1
]}

Chionne, A ^{[1
]}

DAchille, R ^{[1
]}

Bonini, C ^{[1
]}

机构：

[1] UNIV BASILICATA,DIPARTIMENTO CHIM,I-85100 POTENZA,ITALY

来源：

TETRAHEDRON-ASYMMETRY | 1997年 / 8卷 / 06期

关键词：

ASYMMETRIC-SYNTHESIS; MICROGININ; COMPONENT; ESTERS;

D O I：

10.1016/S0957-4166(97)00056-6

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Regio and stereoselective opening of three membered rings by metal halides was utilized for the enantioselective synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid and (3R)-3-aminodecanoic acid. (C) 1997 Published by Elsevier Science Ltd.

引用

页码：903 / 907

页数：5

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