Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate

In the title compound, C(20)H(19)NO(6)S, the phenyl ring of the phenyl­sulfonyl group makes a dihedral angle of 83.35 (5)° with the indole ring system. The mol­ecular structure exhibits a number of short intramolecular C—H⋯O contacts.

Detalles Bibliográficos
Autores principales: Gunasekaran, B., Sureshbabu, Radhakrishnan, Mohanakrishnan, A. K., Chakkaravarthi, G., 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/PMC2970018/
https://www.ncbi.nlm.nih.gov/pubmed/21577492
http://dx.doi.org/10.1107/S1600536809029985
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author Gunasekaran, B.
Sureshbabu, Radhakrishnan
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_facet Gunasekaran, B.
Sureshbabu, Radhakrishnan
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
author_sort Gunasekaran, B.
collection PubMed
description In the title compound, C(20)H(19)NO(6)S, the phenyl ring of the phenyl­sulfonyl group makes a dihedral angle of 83.35 (5)° with the indole ring system. The mol­ecular structure exhibits a number of short intramolecular C—H⋯O contacts.
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spelling pubmed-29700182010-12-30 Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate Gunasekaran, B. Sureshbabu, Radhakrishnan Mohanakrishnan, A. K. Chakkaravarthi, G. Manivannan, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(19)NO(6)S, the phenyl ring of the phenyl­sulfonyl group makes a dihedral angle of 83.35 (5)° with the indole ring system. The mol­ecular structure exhibits a number of short intramolecular C—H⋯O contacts. International Union of Crystallography 2009-08-08 /pmc/articles/PMC2970018/ /pubmed/21577492 http://dx.doi.org/10.1107/S1600536809029985 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.
Sureshbabu, Radhakrishnan
Mohanakrishnan, A. K.
Chakkaravarthi, G.
Manivannan, V.
Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_full Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_fullStr Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_full_unstemmed Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_short Ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1H-indole-3-carboxyl­ate
title_sort ethyl 2-acetoxy­methyl-1-phenyl­sulfonyl-1h-indole-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970018/
https://www.ncbi.nlm.nih.gov/pubmed/21577492
http://dx.doi.org/10.1107/S1600536809029985
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AT mohanakrishnanak ethyl2acetoxymethyl1phenylsulfonyl1hindole3carboxylate
AT chakkaravarthig ethyl2acetoxymethyl1phenylsulfonyl1hindole3carboxylate
AT manivannanv ethyl2acetoxymethyl1phenylsulfonyl1hindole3carboxylate

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