A NEW ROUTE TO OXAZOLIDINONES

被引：10

作者：

DELAUNAY, D ^{[1
]}

LECORRE, M ^{[1
]}

机构：

[1] UNIV RENNES 1,CNRS,SYNTH ORGAN LAB,F-35042 RENNES,FRANCE

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1994年 / 20期

关键词：

D O I：

10.1039/p19940003041

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The oxazolidinones 5 and 7 have been prepared by coupling Grignard, reagents with N-alkoxy-carbonyl-alpha-amino esters. Hydrolysis of oxazolidinones 5 afforded beta-amino alcohols with god yield and enantiomeric excess.

引用

页码：3041 / 3042

页数：2

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