Easy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivative

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dc.contributor.authorDiaz, Gaspar
dc.contributor.authorFreitas, Michelle A. A. de
dc.contributor.authorRicci-Silva, Maria E.
dc.contributor.authorDiaz, Marisa A. N.
dc.date.accessioned2017-10-31T09:49:09Z
dc.date.available2017-10-31T09:49:09Z
dc.date.issued2014-06-06
dc.description.abstractAn 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.en
dc.formatpdfpt-BR
dc.identifier.issn1420-3049
dc.identifier.urihttp://dx.doi.org/10.3390/molecules19067429
dc.identifier.urihttp://www.locus.ufv.br/handle/123456789/12568
dc.language.isoengpt-BR
dc.publisherMoleculespt-BR
dc.relation.ispartofseries19(6), p.7429-7439, June 2014pt-BR
dc.rightsOpen Accesspt-BR
dc.subjectEvans’ oxazolidinonespt-BR
dc.subjectStereoselective synthesispt-BR
dc.subjectMorita-baylis-hillman adductpt-BR
dc.subjectStaphylococcus aureuspt-BR
dc.subjectMastitis bovinapt-BR
dc.titleEasy access to evans’ oxazolidinones. Stereoselective synthesis and antibacterial activity of a new 2-oxazolidinone derivativeen
dc.typeArtigopt-BR

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