Stereoselective Synthesis of -Amino-C-phosphinic Acids and Derivatives

被引:32
|
作者
Luis Viveros-Ceballos, Jose [1 ]
Ordonez, Mario [2 ]
Sayago, Francisco J. [3 ]
Cativiela, Carlos [3 ]
机构
[1] Univ Autonoma Estado Morelos, Secretaria Acad, Ave Univ 1001, Cuernavaca 62209, Morelos, Mexico
[2] Univ Autonoma Estado Morelos, Ctr Invest Quim IICBA, Ave Univ 1001, Cuernavaca 62209, Morelos, Mexico
[3] Univ Zaragoza, Dept Quim Organ, ISQCH, CSIC, E-50009 Zaragoza, Spain
来源
MOLECULES | 2016年 / 21卷 / 09期
关键词
alpha-amino-C-phosphinic acids; alpha-amino-C-phosphinates; alpha-amino acids; stereoselective synthesis; biological activity; ALPHA-AMINOPHOSPHONIC ACIDS; ANGIOTENSIN-CONVERTING ENZYME; ORGANOPHOSPHORUS INHIBITORS; ANALOGS; DESIGN; AMINOPEPTIDASE; PEPTIDES; DIVERSIFICATION; PHOSPHONATES; TRIPEPTIDES;
D O I
10.3390/molecules21091141
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
alpha-Amino-C-phosphinic acids and derivatives are an important group of compounds of synthetic and medicinal interest and particular attention has been dedicated to their stereoselective synthesis in recent years. Among these, phosphinic pseudopeptides have acquired pharmacological importance in influencing physiologic and pathologic processes, primarily acting as inhibitors for proteolytic enzymes where molecular stereochemistry has proven to be critical. This review summarizes the latest developments in the asymmetric synthesis of acyclic and phosphacyclic -amino-C-phosphinic acids and derivatives, following in the first case an order according to the strategy used, whereas for cyclic compounds the nitrogen embedding in the heterocyclic core is considered. In addition selected examples of pharmacological implications of title compounds are also disclosed.
引用
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页数:31
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