Diastereoselective synthesis of (1S,2S,3R,4R) and (1R,2S,3R,4S)-bicyclo[2.2.1]hept-2-amino-2,3-dicarboxylic acids: New conformationally-constrained (S)-aspartic acid analogues

被引：16

作者：

Bunuel, E ^{[1
]}

Cativiela, C ^{[1
]}

DiazdeVillegas, MD ^{[1
]}

机构：

[1] UNIV ZARAGOZA,CSIC,DEPT QUIM ORGAN,INST CIENCIA MAT ARAGON,E-50009 ZARAGOZA,SPAIN

来源：

TETRAHEDRON-ASYMMETRY | 1996年 / 7卷 / 05期

关键词：

D O I：

10.1016/0957-4166(96)00172-3

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The title compounds were prepared from key intermediates readily obtained by the stereoselective Diels-Alder reaction of (Z)-2-phenyl-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-ylmethylene]-5(4H)-oxazolone, a chiral az-lactone derived from (R)-glyceraldehyde and cyclopentadiene. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：1521 / 1528

页数：8

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