Easy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivative
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | LOCUS Repositório Institucional da UFV |
Texto Completo: | http://dx.doi.org/10.3390/molecules19067429 http://www.locus.ufv.br/handle/123456789/12568 |
Resumo: | 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. |
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LOCUS Repositório Institucional da UFV |
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Easy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivativeEvans’ oxazolidinonesStereoselective synthesisMorita-baylis-hillman adductStaphylococcus aureusMastitis bovinaAn 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.Molecules2017-10-31T09:49:09Z2017-10-31T09:49:09Z2014-06-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlepdfapplication/pdf1420-3049http://dx.doi.org/10.3390/molecules19067429http://www.locus.ufv.br/handle/123456789/12568eng19(6), p.7429-7439, June 2014Diaz, GasparFreitas, Michelle A. A. deRicci-Silva, Maria E.Diaz, Marisa A. N.info:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFV2024-07-12T06:53:10Zoai:locus.ufv.br:123456789/12568Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452024-07-12T06:53:10LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false |
dc.title.none.fl_str_mv |
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 |
spellingShingle |
Easy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivative Diaz, Gaspar Evans’ oxazolidinones Stereoselective synthesis Morita-baylis-hillman adduct Staphylococcus aureus Mastitis bovina |
title_short |
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_sort |
Easy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivative |
author |
Diaz, Gaspar |
author_facet |
Diaz, Gaspar Freitas, Michelle A. A. de Ricci-Silva, Maria E. Diaz, Marisa A. N. |
author_role |
author |
author2 |
Freitas, Michelle A. A. de Ricci-Silva, Maria E. Diaz, Marisa A. N. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Diaz, Gaspar Freitas, Michelle A. A. de Ricci-Silva, Maria E. Diaz, Marisa A. N. |
dc.subject.por.fl_str_mv |
Evans’ oxazolidinones Stereoselective synthesis Morita-baylis-hillman adduct Staphylococcus aureus Mastitis bovina |
topic |
Evans’ oxazolidinones Stereoselective synthesis Morita-baylis-hillman adduct Staphylococcus aureus Mastitis bovina |
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. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-06-06 2017-10-31T09:49:09Z 2017-10-31T09:49:09Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
1420-3049 http://dx.doi.org/10.3390/molecules19067429 http://www.locus.ufv.br/handle/123456789/12568 |
identifier_str_mv |
1420-3049 |
url |
http://dx.doi.org/10.3390/molecules19067429 http://www.locus.ufv.br/handle/123456789/12568 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
19(6), p.7429-7439, June 2014 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
pdf application/pdf |
dc.publisher.none.fl_str_mv |
Molecules |
publisher.none.fl_str_mv |
Molecules |
dc.source.none.fl_str_mv |
reponame:LOCUS Repositório Institucional da UFV instname:Universidade Federal de Viçosa (UFV) instacron:UFV |
instname_str |
Universidade Federal de Viçosa (UFV) |
instacron_str |
UFV |
institution |
UFV |
reponame_str |
LOCUS Repositório Institucional da UFV |
collection |
LOCUS Repositório Institucional da UFV |
repository.name.fl_str_mv |
LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV) |
repository.mail.fl_str_mv |
fabiojreis@ufv.br |
_version_ |
1822610585811943424 |