RESOLUTION AND REGIOSELECTIVE PROTECTION OF GLUTAMIC-ACID ANALOGS .1. RESOLUTION OF DIASTEREOMERIC ALPHA-BOROXAZOLIDONE DERIVATIVES

被引：23

作者：

ACHER, F ^{[1
]}

AZERAD, R ^{[1
]}

机构：

[1] UNIV PARIS 05,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,CNRS,UNITE ASSOCIEE 400,F-75270 PARIS 06,FRANCE

来源：

TETRAHEDRON-ASYMMETRY | 1994年 / 5卷 / 04期

关键词：

D O I：

10.1016/0957-4166(94)80036-7

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Diastereomeric alpha-boroxazolidone gamma-phenylethylamide (or gamma-phenylethanolamide) derivatives of 2-, 3- or 4-substituted glutamic acid analogues have been separated by silicagel chromatography, resulting, after deprotection, in a practical method for the resolution of most of these unnatural amino acids.

引用

页码：731 / 744

页数：14

共 95 条

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