Recent progress on the stereoselective synthesis of cyclic quaternary α-amino acids

被引：203
|
作者：
Cativiela, Carlos [1 ]
Ordonez, Mario [2 ]
机构：
[1] Univ Zaragoza, CSIC, Dept Quim Organ, ICMA, E-50009 Zaragoza, Spain
[2] Univ Autonoma Estado Morelos, Ctr Invest Quim, Cuernavaca 62209, Morelos, Mexico
来源：
TETRAHEDRON-ASYMMETRY | 2009年 / 20卷 / 01期
基金：
美国国家卫生研究院;
关键词：
ASYMMETRIC STRECKER SYNTHESIS; ALDOSE REDUCTASE INHIBITORS; INDUCED AXIAL CHIRALITY; CYCLOALIPHATIC C-ALPHA; C-ALPHA-DISUBSTITUTED GLYCINE; 1,3-DIPOLAR CYCLOADDITION REACTIONS; METABOTROPIC GLUTAMATE RECEPTORS; CONSTRAINED CYCLOPROPANE ANALOG; OLEFIN-METATHESIS CATALYSTS; TRANSITION-METAL RECEPTOR; RING CLOSING METATHESIS;
D O I：
10.1016/j.tetasy.2009.01.002
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
The most recent papers describing the stereoselective synthesis of cyclic quaternary alpha-amino acids are collected in this review. The diverse synthetic approaches are classified according to the size of the ring and taking into account the bond that is formed to complete the quaternary skeleton. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码：1 / 63
页数：63
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