exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione

The title compound, C16H15NO3, consists of an oxabicycle fused to an N-phenyl-substituted pyrrolidine ring anti to the double bond, affording the exo isomer. In the oxabicycle system, the six-membered ring presents a boat conformation, while the heterocyclic rings show envelope conformations with th...

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Main Authors: Pineda-Contreras, Armando, Vázquez-Vuelvas, Oscar Fernando, Negrete-López, Laura Edith, García-Ortega, Héctor, Flores-Alamo, Marcos
Format: Online
Language:English
Published: International Union of Crystallography 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885034/
id pubmed-3885034
recordtype oai_dc
spelling pubmed-38850342014-01-17 exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione Pineda-Contreras, Armando Vázquez-Vuelvas, Oscar Fernando Negrete-López, Laura Edith García-Ortega, Héctor Flores-Alamo, Marcos Organic Papers The title compound, C16H15NO3, consists of an oxabicycle fused to an N-phenyl-substituted pyrrolidine ring anti to the double bond, affording the exo isomer. In the oxabicycle system, the six-membered ring presents a boat conformation, while the heterocyclic rings show envelope conformations with the O atom projected out of the plane. In the crystal, adjacent mol­ecules are linked via weak C—H⋯O hydrogen bonds, forming chains propagating along the a-axis direction. The chains are linked by C—H⋯π inter­actions, forming two-dimensional networks lying parallel to the ac plane. International Union of Crystallography 2013-11-09 /pmc/articles/PMC3885034/ /pubmed/24454209 http://dx.doi.org/10.1107/S1600536813030262 Text en © Pineda-Contreras et al. 2013 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.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Pineda-Contreras, Armando
Vázquez-Vuelvas, Oscar Fernando
Negrete-López, Laura Edith
García-Ortega, Héctor
Flores-Alamo, Marcos
spellingShingle Pineda-Contreras, Armando
Vázquez-Vuelvas, Oscar Fernando
Negrete-López, Laura Edith
García-Ortega, Héctor
Flores-Alamo, Marcos
exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
author_facet Pineda-Contreras, Armando
Vázquez-Vuelvas, Oscar Fernando
Negrete-López, Laura Edith
García-Ortega, Héctor
Flores-Alamo, Marcos
author_sort Pineda-Contreras, Armando
title exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
title_short exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
title_full exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
title_fullStr exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
title_full_unstemmed exo-1,7-Dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
title_sort exo-1,7-dimethyl-4-phenyl-10-oxa-4-aza­tri­cyclo­[5.2.1.02,6]dec-8-ene-3,5-dione
description The title compound, C16H15NO3, consists of an oxabicycle fused to an N-phenyl-substituted pyrrolidine ring anti to the double bond, affording the exo isomer. In the oxabicycle system, the six-membered ring presents a boat conformation, while the heterocyclic rings show envelope conformations with the O atom projected out of the plane. In the crystal, adjacent mol­ecules are linked via weak C—H⋯O hydrogen bonds, forming chains propagating along the a-axis direction. The chains are linked by C—H⋯π inter­actions, forming two-dimensional networks lying parallel to the ac plane.
publisher International Union of Crystallography
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885034/
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