(R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one

The title compound, C(21)H(25)NO(2)S, consists of a five-membered heterocyclic ring, with pendant phenyl groups, an isopropyl group and a thio­ether residue. The thio­ether bonds to the heterocycle via the N atom. The absolute configuration results from an inversion of the configuration of substrate...

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Detalles Bibliográficos
Autores principales: Pozza Silveira, Gustavo, Bonfante de Carvallho, Cassandra, Oliver, Allen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393316/
https://www.ncbi.nlm.nih.gov/pubmed/22807873
http://dx.doi.org/10.1107/S160053681202569X
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author Pozza Silveira, Gustavo
Bonfante de Carvallho, Cassandra
Oliver, Allen
author_facet Pozza Silveira, Gustavo
Bonfante de Carvallho, Cassandra
Oliver, Allen
author_sort Pozza Silveira, Gustavo
collection PubMed
description The title compound, C(21)H(25)NO(2)S, consists of a five-membered heterocyclic ring, with pendant phenyl groups, an isopropyl group and a thio­ether residue. The thio­ether bonds to the heterocycle via the N atom. The absolute configuration results from an inversion of the configuration of substrate during the synthesis.
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spelling pubmed-33933162012-07-17 (R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one Pozza Silveira, Gustavo Bonfante de Carvallho, Cassandra Oliver, Allen Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(25)NO(2)S, consists of a five-membered heterocyclic ring, with pendant phenyl groups, an isopropyl group and a thio­ether residue. The thio­ether bonds to the heterocycle via the N atom. The absolute configuration results from an inversion of the configuration of substrate during the synthesis. International Union of Crystallography 2012-06-13 /pmc/articles/PMC3393316/ /pubmed/22807873 http://dx.doi.org/10.1107/S160053681202569X Text en © Pozza Silveira et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Pozza Silveira, Gustavo
Bonfante de Carvallho, Cassandra
Oliver, Allen
(R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
title (R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
title_full (R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
title_fullStr (R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
title_full_unstemmed (R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
title_short (R)-4-Isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
title_sort (r)-4-isopropyl-3-isopropyl­sulfanyl-5,5-diphenyl-1,3-oxazolidin-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393316/
https://www.ncbi.nlm.nih.gov/pubmed/22807873
http://dx.doi.org/10.1107/S160053681202569X
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