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Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate

The title compound, C(20)H(29)NO(6)S, crystallizes with two mol­ecules in the asymmetric unit, with similar conformations. The dioxane and pyridine rings adopt twist conformations in both mol­ecules. The packing is stabilized by inter­molecular C—H⋯O hydrogen bonds.

Detalles Bibliográficos
Autores principales: Selvanayagam, S., Sridhar, B., Ravikumar, K., Kathiravan, S., Raghunathan, R.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977770/
https://www.ncbi.nlm.nih.gov/pubmed/21583906
http://dx.doi.org/10.1107/S1600536809014391
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author Selvanayagam, S.
Sridhar, B.
Ravikumar, K.
Kathiravan, S.
Raghunathan, R.
author_facet Selvanayagam, S.
Sridhar, B.
Ravikumar, K.
Kathiravan, S.
Raghunathan, R.
author_sort Selvanayagam, S.
collection PubMed
description The title compound, C(20)H(29)NO(6)S, crystallizes with two mol­ecules in the asymmetric unit, with similar conformations. The dioxane and pyridine rings adopt twist conformations in both mol­ecules. The packing is stabilized by inter­molecular C—H⋯O hydrogen bonds.
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spelling pubmed-29777702010-12-30 Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate Selvanayagam, S. Sridhar, B. Ravikumar, K. Kathiravan, S. Raghunathan, R. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(29)NO(6)S, crystallizes with two mol­ecules in the asymmetric unit, with similar conformations. The dioxane and pyridine rings adopt twist conformations in both mol­ecules. The packing is stabilized by inter­molecular C—H⋯O hydrogen bonds. International Union of Crystallography 2009-04-22 /pmc/articles/PMC2977770/ /pubmed/21583906 http://dx.doi.org/10.1107/S1600536809014391 Text en © Selvanayagam 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
Selvanayagam, S.
Sridhar, B.
Ravikumar, K.
Kathiravan, S.
Raghunathan, R.
Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
title Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
title_full Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
title_fullStr Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
title_full_unstemmed Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
title_short Methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
title_sort methyl 2-(2,2,4-trimethyl-6-tosyl­perhydro-1,3-dioxino[5,4-c]pyridin-5-yl)acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977770/
https://www.ncbi.nlm.nih.gov/pubmed/21583906
http://dx.doi.org/10.1107/S1600536809014391
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