Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate

The title steroid, C(29)H(44)O(7), is a new androgen derivative and a key inter­mediate for synthesizing novel anti-HIV steroid agents. There are four trans-fused rings in the structure. The three six-membered rings exhibit chair conformations, while the five-membered ring adopts an envelope conform...

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Detalles Bibliográficos
Autores principales: Yan, Xin, Xu, Shiqing, Wang, Jingmei, Chen, Ying, Xia, Peng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969632/
https://www.ncbi.nlm.nih.gov/pubmed/21583145
http://dx.doi.org/10.1107/S1600536809017243
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author Yan, Xin
Xu, Shiqing
Wang, Jingmei
Chen, Ying
Xia, Peng
author_facet Yan, Xin
Xu, Shiqing
Wang, Jingmei
Chen, Ying
Xia, Peng
author_sort Yan, Xin
collection PubMed
description The title steroid, C(29)H(44)O(7), is a new androgen derivative and a key inter­mediate for synthesizing novel anti-HIV steroid agents. There are four trans-fused rings in the structure. The three six-membered rings exhibit chair conformations, while the five-membered ring adopts an envelope conformation.
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spelling pubmed-29696322010-12-30 Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate Yan, Xin Xu, Shiqing Wang, Jingmei Chen, Ying Xia, Peng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title steroid, C(29)H(44)O(7), is a new androgen derivative and a key inter­mediate for synthesizing novel anti-HIV steroid agents. There are four trans-fused rings in the structure. The three six-membered rings exhibit chair conformations, while the five-membered ring adopts an envelope conformation. International Union of Crystallography 2009-05-14 /pmc/articles/PMC2969632/ /pubmed/21583145 http://dx.doi.org/10.1107/S1600536809017243 Text en © Yan 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
Yan, Xin
Xu, Shiqing
Wang, Jingmei
Chen, Ying
Xia, Peng
Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
title Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
title_full Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
title_fullStr Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
title_full_unstemmed Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
title_short Methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
title_sort methyl 3β-methoxy­carbon­yloxy-4,4-di­methyl-17-oxo-16α-(3-oxobut­yl)-16β-carboxylate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969632/
https://www.ncbi.nlm.nih.gov/pubmed/21583145
http://dx.doi.org/10.1107/S1600536809017243
work_keys_str_mv AT yanxin methyl3bmethoxycarbonyloxy44dimethyl17oxo16a3oxobutyl16bcarboxylate
AT xushiqing methyl3bmethoxycarbonyloxy44dimethyl17oxo16a3oxobutyl16bcarboxylate
AT wangjingmei methyl3bmethoxycarbonyloxy44dimethyl17oxo16a3oxobutyl16bcarboxylate
AT chenying methyl3bmethoxycarbonyloxy44dimethyl17oxo16a3oxobutyl16bcarboxylate
AT xiapeng methyl3bmethoxycarbonyloxy44dimethyl17oxo16a3oxobutyl16bcarboxylate

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