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(1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate

In the title mol­ecule, C(25)H(30)O(4), the napthalene ring system is slightly bowed, with a dihedral angle of 4.37 (13)° between the two benzene rings.

Detalles Bibliográficos
Autores principales: Lough, Alan J., Petrone, David A., Tam, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151886/
https://www.ncbi.nlm.nih.gov/pubmed/21837213
http://dx.doi.org/10.1107/S1600536811024238
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author Lough, Alan J.
Petrone, David A.
Tam, William
author_facet Lough, Alan J.
Petrone, David A.
Tam, William
author_sort Lough, Alan J.
collection PubMed
description In the title mol­ecule, C(25)H(30)O(4), the napthalene ring system is slightly bowed, with a dihedral angle of 4.37 (13)° between the two benzene rings.
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spelling pubmed-31518862011-08-11 (1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate Lough, Alan J. Petrone, David A. Tam, William Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(25)H(30)O(4), the napthalene ring system is slightly bowed, with a dihedral angle of 4.37 (13)° between the two benzene rings. International Union of Crystallography 2011-06-30 /pmc/articles/PMC3151886/ /pubmed/21837213 http://dx.doi.org/10.1107/S1600536811024238 Text en © Lough et al. 2011 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
Lough, Alan J.
Petrone, David A.
Tam, William
(1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
title (1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
title_full (1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
title_fullStr (1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
title_full_unstemmed (1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
title_short (1S,2S,4R)-7-tert-But­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
title_sort (1s,2s,4r)-7-tert-but­oxy­bicyclo­[2.2.1]hept-5-en-2-yl (2s)-2-(6-meth­oxy­naphthalen-2-yl)propano­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151886/
https://www.ncbi.nlm.nih.gov/pubmed/21837213
http://dx.doi.org/10.1107/S1600536811024238
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