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

机译:立体选择性合成α-氨基-C-次膦酸及其衍生物

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摘要

α-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 α-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.
机译:α-氨基-C-次膦酸及其衍生物是合成和医学上重要的一组化合物,并且近年来特别关注其立体选择性合成。其中,次膦酸假肽在影响生理和病理过程中具有药理学重要性,主要用作蛋白水解酶的抑制剂,而分子立体化学已被证明是至关重要的。这篇综述总结了无环和磷环α-氨基-C-次膦酸及其衍生物的不对称合成的最新进展,在第一种情况下,根据所使用的策略按顺序排列,而对于环状化合物,氮嵌入杂环核中是考虑过的。另外,还公开了标题化合物的药理意义的选定实例。

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