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(3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one

Mol­ecules of the title compound [systematic name: (2R,5S,7S)-2-phenyl-7-phenyl­sulfanyl-1-aza-3-oxa­bicyclo­[3.3.0]octan-8-one], C(18)H(17)NO(2)S, form high quality crystals even though they are only packed using C—H⋯O(carbon­yl) and weak C—H⋯S inter­actions. The dihedral angle between the aromatic...

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Detalles Bibliográficos
Autores principales: Gainsford, Graeme J., Luxenburger, Andreas, Woolhouse, Anthony D.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977644/
https://www.ncbi.nlm.nih.gov/pubmed/21583987
http://dx.doi.org/10.1107/S1600536809011623
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author Gainsford, Graeme J.
Luxenburger, Andreas
Woolhouse, Anthony D.
author_facet Gainsford, Graeme J.
Luxenburger, Andreas
Woolhouse, Anthony D.
author_sort Gainsford, Graeme J.
collection PubMed
description Mol­ecules of the title compound [systematic name: (2R,5S,7S)-2-phenyl-7-phenyl­sulfanyl-1-aza-3-oxa­bicyclo­[3.3.0]octan-8-one], C(18)H(17)NO(2)S, form high quality crystals even though they are only packed using C—H⋯O(carbon­yl) and weak C—H⋯S inter­actions. The dihedral angle between the aromatic rings is 85.53 (5)°. The fused rings adopt envelope and twist conformations.
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spelling pubmed-29776442010-12-30 (3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one Gainsford, Graeme J. Luxenburger, Andreas Woolhouse, Anthony D. Acta Crystallogr Sect E Struct Rep Online Organic Papers Mol­ecules of the title compound [systematic name: (2R,5S,7S)-2-phenyl-7-phenyl­sulfanyl-1-aza-3-oxa­bicyclo­[3.3.0]octan-8-one], C(18)H(17)NO(2)S, form high quality crystals even though they are only packed using C—H⋯O(carbon­yl) and weak C—H⋯S inter­actions. The dihedral angle between the aromatic rings is 85.53 (5)°. The fused rings adopt envelope and twist conformations. International Union of Crystallography 2009-04-02 /pmc/articles/PMC2977644/ /pubmed/21583987 http://dx.doi.org/10.1107/S1600536809011623 Text en © Gainsford et al. 2009 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
Gainsford, Graeme J.
Luxenburger, Andreas
Woolhouse, Anthony D.
(3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
title (3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
title_full (3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
title_fullStr (3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
title_full_unstemmed (3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
title_short (3R,6S,7aS)-3-Phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
title_sort (3r,6s,7as)-3-phenyl-6-(phenyl­sulfan­yl)perhydro­pyrrolo[1,2-c]oxazol-5-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977644/
https://www.ncbi.nlm.nih.gov/pubmed/21583987
http://dx.doi.org/10.1107/S1600536809011623
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