Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate

In the title compound, C(24)H(23)NO(3), the dihedral angle between the naphthalene ring system and the phenyl ring is 76.82 (6)°. The pyrrolidine ring adopts an envelope conformation. In the crystal, weak inter­molecular C—H⋯O and C—H⋯π inter­actions are observed.

Detalles Bibliográficos
Autores principales: Gunasekaran, B., Kathiravan, S., Raghunathan, R., Renuga, V., Manivannan, V.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977716/
https://www.ncbi.nlm.nih.gov/pubmed/21583852
http://dx.doi.org/10.1107/S1600536809012914
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author Gunasekaran, B.
Kathiravan, S.
Raghunathan, R.
Renuga, V.
Manivannan, V.
author_facet Gunasekaran, B.
Kathiravan, S.
Raghunathan, R.
Renuga, V.
Manivannan, V.
author_sort Gunasekaran, B.
collection PubMed
description In the title compound, C(24)H(23)NO(3), the dihedral angle between the naphthalene ring system and the phenyl ring is 76.82 (6)°. The pyrrolidine ring adopts an envelope conformation. In the crystal, weak inter­molecular C—H⋯O and C—H⋯π inter­actions are observed.
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spelling pubmed-29777162010-12-30 Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate Gunasekaran, B. Kathiravan, S. Raghunathan, R. Renuga, V. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(24)H(23)NO(3), the dihedral angle between the naphthalene ring system and the phenyl ring is 76.82 (6)°. The pyrrolidine ring adopts an envelope conformation. In the crystal, weak inter­molecular C—H⋯O and C—H⋯π inter­actions are observed. International Union of Crystallography 2009-04-10 /pmc/articles/PMC2977716/ /pubmed/21583852 http://dx.doi.org/10.1107/S1600536809012914 Text en © Gunasekaran 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
Gunasekaran, B.
Kathiravan, S.
Raghunathan, R.
Renuga, V.
Manivannan, V.
Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
title Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
title_full Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
title_fullStr Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
title_full_unstemmed Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
title_short Methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
title_sort methyl 1-methyl-3-phenyl-1,2,3,3a,4,9b-hexa­hydro­benzo[f]chromeno[4,3-b]pyrrole-3a-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977716/
https://www.ncbi.nlm.nih.gov/pubmed/21583852
http://dx.doi.org/10.1107/S1600536809012914
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