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

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 influe...

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Autores principales: Viveros-Ceballos, José Luis, Ordóñez, Mario, Sayago, Francisco J., Cativiela, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274224/
https://www.ncbi.nlm.nih.gov/pubmed/27589703
http://dx.doi.org/10.3390/molecules21091141
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author Viveros-Ceballos, José Luis
Ordóñez, Mario
Sayago, Francisco J.
Cativiela, Carlos
author_facet Viveros-Ceballos, José Luis
Ordóñez, Mario
Sayago, Francisco J.
Cativiela, Carlos
author_sort Viveros-Ceballos, José Luis
collection PubMed
description 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.
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spelling pubmed-62742242018-12-28 Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives Viveros-Ceballos, José Luis Ordóñez, Mario Sayago, Francisco J. Cativiela, Carlos Molecules Review 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. MDPI 2016-08-29 /pmc/articles/PMC6274224/ /pubmed/27589703 http://dx.doi.org/10.3390/molecules21091141 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Viveros-Ceballos, José Luis
Ordóñez, Mario
Sayago, Francisco J.
Cativiela, Carlos
Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives
title Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives
title_full Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives
title_fullStr Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives
title_full_unstemmed Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives
title_short Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives
title_sort stereoselective synthesis of α-amino-c-phosphinic acids and derivatives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274224/
https://www.ncbi.nlm.nih.gov/pubmed/27589703
http://dx.doi.org/10.3390/molecules21091141
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