DIASTEREOSELECTIVE RADICAL-ADDITION TO METHYLENEOXAZOLIDINONES - AN ENANTIOSELECTIVE ROUTE TO ALPHA-AMINO-ACIDS

被引：86

作者：

AXON, JR ^{[1
]}

BECKWITH, ALJ ^{[1
]}

机构：

[1] AUSTRALIAN NATL UNIV,RES SCH CHEM,INST ADV STUDIES,CANBERRA,ACT 0200,AUSTRALIA

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1995年 / 05期

关键词：

D O I：

10.1039/c39950000549

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The diastereoselectivity of radical addition to methyleneoxazolidinones depends on the nature of the addend radical and of the N-protecting group; the reaction provides a convenient enantioselective route to alpha-amino acids.

引用

页码：549 / 550

页数：2

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