tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate

In the title compound, C(22)H(26)BrNO(6), the indole ring system is planar [maximum deviation 0.029 (2) Å]. The tert-butyl bound carboxyl­ate group forms a dihedral angle of 17.54 (8)° with the indole ring system. In the crystal, mol­ecules are linked into centrosymmetric R (2) (2)(10) dimers by pai...

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Detalles Bibliográficos
Autores principales: Thenmozhi, M., Kavitha, T., Dhayalan, V., Mohanakrishnan, A. K., Ponnuswamy, M. N.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971097/
https://www.ncbi.nlm.nih.gov/pubmed/21578388
http://dx.doi.org/10.1107/S1600536809041567
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author Thenmozhi, M.
Kavitha, T.
Dhayalan, V.
Mohanakrishnan, A. K.
Ponnuswamy, M. N.
author_facet Thenmozhi, M.
Kavitha, T.
Dhayalan, V.
Mohanakrishnan, A. K.
Ponnuswamy, M. N.
author_sort Thenmozhi, M.
collection PubMed
description In the title compound, C(22)H(26)BrNO(6), the indole ring system is planar [maximum deviation 0.029 (2) Å]. The tert-butyl bound carboxyl­ate group forms a dihedral angle of 17.54 (8)° with the indole ring system. In the crystal, mol­ecules are linked into centrosymmetric R (2) (2)(10) dimers by paired C—H⋯O hydrogen bonds.
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spelling pubmed-29710972010-12-30 tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate Thenmozhi, M. Kavitha, T. Dhayalan, V. Mohanakrishnan, A. K. Ponnuswamy, M. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(22)H(26)BrNO(6), the indole ring system is planar [maximum deviation 0.029 (2) Å]. The tert-butyl bound carboxyl­ate group forms a dihedral angle of 17.54 (8)° with the indole ring system. In the crystal, mol­ecules are linked into centrosymmetric R (2) (2)(10) dimers by paired C—H⋯O hydrogen bonds. International Union of Crystallography 2009-10-17 /pmc/articles/PMC2971097/ /pubmed/21578388 http://dx.doi.org/10.1107/S1600536809041567 Text en © Thenmozhi 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
Thenmozhi, M.
Kavitha, T.
Dhayalan, V.
Mohanakrishnan, A. K.
Ponnuswamy, M. N.
tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate
title tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate
title_full tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate
title_fullStr tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate
title_full_unstemmed tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate
title_short tert-Butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1H-indole-1-carboxyl­ate
title_sort tert-butyl 3-[2,2-bis­(ethoxy­carbon­yl)vin­yl]-2-bromo­methyl-1h-indole-1-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971097/
https://www.ncbi.nlm.nih.gov/pubmed/21578388
http://dx.doi.org/10.1107/S1600536809041567
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AT kavithat tertbutyl322bisethoxycarbonylvinyl2bromomethyl1hindole1carboxylate
AT dhayalanv tertbutyl322bisethoxycarbonylvinyl2bromomethyl1hindole1carboxylate
AT mohanakrishnanak tertbutyl322bisethoxycarbonylvinyl2bromomethyl1hindole1carboxylate
AT ponnuswamymn tertbutyl322bisethoxycarbonylvinyl2bromomethyl1hindole1carboxylate

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