Stereoselective Synthesis of α-Aminophosphonic Acids Analogs of the 20 Proteinogenic α-Amino Acids

被引：58
作者：
Ordonez, Mario [1 ]
Luis Viveros-Ceballos, Jose [1 ]
Cativiela, Carlos [2 ]
Arizpe, Alicia [2 ]
机构：
[1] Univ Autonoma Estado Morelos, Ctr Invest Quim, Cuernavaca 62209, Morelos, Mexico
[2] Univ Zaragoza, CSIC, ICMA, Dept Quim Organ, E-50009 Zaragoza, Spain
来源：
CURRENT ORGANIC SYNTHESIS | 2012年 / 9卷 / 03期
关键词：
alpha-Aminophosphonic acids; alpha-aminophosphonates; alpha-amino acids; stereoselective synthesis; biological activity; resolution; I-CONVERTING-ENZYME; TRANSITION-STATE ANALOG; ACTIVE 1-AMINOALKANEPHOSPHONIC ACIDS; CATALYTIC ASYMMETRIC-SYNTHESIS; LACTAMASE-INHIBITORY ACTIVITY; HUMAN NEUTROPHIL COLLAGENASE; ORGANIC PHOSPHORUS-COMPOUNDS; L-LEUCINEPHOSPHONIC ACID; SERINE BETA-LACTAMASES; 1-AMINOALKYLPHOSPHONIC ACIDS;
D O I：
10.2174/157017912801270595
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
This review describes the synthesis, biological interest and importance of the alpha-aminophosphonic acids analogs of the 20 proteinogenic alpha-amino acids. Special attention is devoted to those stereoselective procedures that allow the synthesis of the required compounds in enantiomerically pure form.
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收藏
页码：310 / 341
页数：32
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