Cargando…
Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative
An interesting new approach was developed for the synthesis of Evans’ chiral auxiliaries with excellent yields. In turn, another new stereoselective and efficient strategy has also allowed for the preparation of a 2-oxazolidinone derivative in 34% overall yield from the Morita-Baylis-Hillman adduct....
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270906/ https://www.ncbi.nlm.nih.gov/pubmed/24914892 http://dx.doi.org/10.3390/molecules19067429 |
_version_ | 1783376806597885952 |
---|---|
author | Diaz, Gaspar de Freitas, Michelle A. A. Ricci-Silva, Maria E. Diaz, Marisa A. N. |
author_facet | Diaz, Gaspar de Freitas, Michelle A. A. Ricci-Silva, Maria E. Diaz, Marisa A. N. |
author_sort | Diaz, Gaspar |
collection | PubMed |
description | An interesting new approach was developed for the synthesis of Evans’ chiral auxiliaries with excellent yields. In turn, another new stereoselective and efficient strategy has also allowed for the preparation of a 2-oxazolidinone derivative in 34% overall yield from the Morita-Baylis-Hillman adduct. The antibacterial activity of this oxazolidinone was tested against Staphylococcus aureus strains isolated from animals with mastitis infections. |
format | Online Article Text |
id | pubmed-6270906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62709062018-12-21 Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative Diaz, Gaspar de Freitas, Michelle A. A. Ricci-Silva, Maria E. Diaz, Marisa A. N. Molecules Article An interesting new approach was developed for the synthesis of Evans’ chiral auxiliaries with excellent yields. In turn, another new stereoselective and efficient strategy has also allowed for the preparation of a 2-oxazolidinone derivative in 34% overall yield from the Morita-Baylis-Hillman adduct. The antibacterial activity of this oxazolidinone was tested against Staphylococcus aureus strains isolated from animals with mastitis infections. MDPI 2014-06-06 /pmc/articles/PMC6270906/ /pubmed/24914892 http://dx.doi.org/10.3390/molecules19067429 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Diaz, Gaspar de Freitas, Michelle A. A. Ricci-Silva, Maria E. Diaz, Marisa A. N. Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative |
title | Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative |
title_full | Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative |
title_fullStr | Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative |
title_full_unstemmed | Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative |
title_short | Easy Access to Evans’ Oxazolidinones. Stereoselective Synthesis and Antibacterial Activity of a New 2-Oxazolidinone Derivative |
title_sort | easy access to evans’ oxazolidinones. stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivative |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270906/ https://www.ncbi.nlm.nih.gov/pubmed/24914892 http://dx.doi.org/10.3390/molecules19067429 |
work_keys_str_mv | AT diazgaspar easyaccesstoevansoxazolidinonesstereoselectivesynthesisandantibacterialactivityofanew2oxazolidinonederivative AT defreitasmichelleaa easyaccesstoevansoxazolidinonesstereoselectivesynthesisandantibacterialactivityofanew2oxazolidinonederivative AT riccisilvamariae easyaccesstoevansoxazolidinonesstereoselectivesynthesisandantibacterialactivityofanew2oxazolidinonederivative AT diazmarisaan easyaccesstoevansoxazolidinonesstereoselectivesynthesisandantibacterialactivityofanew2oxazolidinonederivative |