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(R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate
(RS)-(±)-2-Methoxycarbonyl-3-tropinone is an important intermediate for the preparation of cocaine and its derivatives. The molecule in the title compound, C(10)H(16)NO(3) (+)·C(4)H(5)O(6) (−), is present as the enol tautomer. The six-membered ring adopts a half boat conformation, and the five-mem...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962227/ https://www.ncbi.nlm.nih.gov/pubmed/21203339 http://dx.doi.org/10.1107/S1600536808023532 |
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author | Yu, Jian-Bing Chen, Shuang-Wei Zheng, Guo-Rong Dai, Li-Yan |
author_facet | Yu, Jian-Bing Chen, Shuang-Wei Zheng, Guo-Rong Dai, Li-Yan |
author_sort | Yu, Jian-Bing |
collection | PubMed |
description | (RS)-(±)-2-Methoxycarbonyl-3-tropinone is an important intermediate for the preparation of cocaine and its derivatives. The molecule in the title compound, C(10)H(16)NO(3) (+)·C(4)H(5)O(6) (−), is present as the enol tautomer. The six-membered ring adopts a half boat conformation, and the five-membered ring a slightly distorted envelope conformation. There are intra- and intermolecular hydrogen bonds involving the hydroxyl, carboxyl groups and quaternary ammonium groups. |
format | Text |
id | pubmed-2962227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29622272010-12-30 (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate Yu, Jian-Bing Chen, Shuang-Wei Zheng, Guo-Rong Dai, Li-Yan Acta Crystallogr Sect E Struct Rep Online Organic Papers (RS)-(±)-2-Methoxycarbonyl-3-tropinone is an important intermediate for the preparation of cocaine and its derivatives. The molecule in the title compound, C(10)H(16)NO(3) (+)·C(4)H(5)O(6) (−), is present as the enol tautomer. The six-membered ring adopts a half boat conformation, and the five-membered ring a slightly distorted envelope conformation. There are intra- and intermolecular hydrogen bonds involving the hydroxyl, carboxyl groups and quaternary ammonium groups. International Union of Crystallography 2008-07-31 /pmc/articles/PMC2962227/ /pubmed/21203339 http://dx.doi.org/10.1107/S1600536808023532 Text en © Yu et al. 2008 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 Yu, Jian-Bing Chen, Shuang-Wei Zheng, Guo-Rong Dai, Li-Yan (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
title | (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
title_full | (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
title_fullStr | (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
title_full_unstemmed | (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
title_short | (R)-(+)-3-Hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
title_sort | (r)-(+)-3-hydroxy-2-methoxycarbonyl-8-methyl-8-azoniabicyclo[3.2.1]octane l-bitartrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962227/ https://www.ncbi.nlm.nih.gov/pubmed/21203339 http://dx.doi.org/10.1107/S1600536808023532 |
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