7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one

In the title compound, C(12)H(13)NO(2), the pyrrolidinone moiety is almost flat while the oxazole ring adopts an envelope conformation with the carbon atom bearing the phenyl substituent as the flap: the angle between the mean planes of the fused heterocyclic rings is 45.47 (19)°. In the crystal, C—...

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Autores principales: Linkova, Elena I., Grinev, Vyacheslav S., Mayorova, Oksana A., Yegorova, Alevtina Yu.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462255/
https://www.ncbi.nlm.nih.gov/pubmed/36339787
http://dx.doi.org/10.1107/S2414314620009190
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author Linkova, Elena I.
Grinev, Vyacheslav S.
Mayorova, Oksana A.
Yegorova, Alevtina Yu.
author_facet Linkova, Elena I.
Grinev, Vyacheslav S.
Mayorova, Oksana A.
Yegorova, Alevtina Yu.
author_sort Linkova, Elena I.
collection PubMed
description In the title compound, C(12)H(13)NO(2), the pyrrolidinone moiety is almost flat while the oxazole ring adopts an envelope conformation with the carbon atom bearing the phenyl substituent as the flap: the angle between the mean planes of the fused heterocyclic rings is 45.47 (19)°. In the crystal, C—H⋯O and C—H⋯π contacts link the mol­ecules into infinite [010] chains. [Image: see text]
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spelling pubmed-94622552022-11-04 7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one Linkova, Elena I. Grinev, Vyacheslav S. Mayorova, Oksana A. Yegorova, Alevtina Yu. IUCrdata Data Reports In the title compound, C(12)H(13)NO(2), the pyrrolidinone moiety is almost flat while the oxazole ring adopts an envelope conformation with the carbon atom bearing the phenyl substituent as the flap: the angle between the mean planes of the fused heterocyclic rings is 45.47 (19)°. In the crystal, C—H⋯O and C—H⋯π contacts link the mol­ecules into infinite [010] chains. [Image: see text] International Union of Crystallography 2020-07-10 /pmc/articles/PMC9462255/ /pubmed/36339787 http://dx.doi.org/10.1107/S2414314620009190 Text en © Linkova et al. 2020 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Linkova, Elena I.
Grinev, Vyacheslav S.
Mayorova, Oksana A.
Yegorova, Alevtina Yu.
7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one
title 7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one
title_full 7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one
title_fullStr 7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one
title_full_unstemmed 7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one
title_short 7a-Phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6H)-one
title_sort 7a-phenyl­tetra­hydro­pyrrolo­[2,1-b]oxazol-5(6h)-one
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462255/
https://www.ncbi.nlm.nih.gov/pubmed/36339787
http://dx.doi.org/10.1107/S2414314620009190
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