17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one

The title compound, C(19)H(28)O(3), the fungal-transformed metabolite of the steroid methyl­oestrenol contains four fused rings A, B, C and D. Ring A adopts a half-chair and the trans-fused rings B and C adopt chair confirmations; the five-membered D ring is folded like an envelope. In the crystal,...

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Detalles Bibliográficos
Autores principales: Yousuf, Sammer, Zafar, Salman, Choudhary, Muhammed Iqbal, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009298/
https://www.ncbi.nlm.nih.gov/pubmed/21589072
http://dx.doi.org/10.1107/S160053681004033X
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author Yousuf, Sammer
Zafar, Salman
Choudhary, Muhammed Iqbal
Ng, Seik Weng
author_facet Yousuf, Sammer
Zafar, Salman
Choudhary, Muhammed Iqbal
Ng, Seik Weng
author_sort Yousuf, Sammer
collection PubMed
description The title compound, C(19)H(28)O(3), the fungal-transformed metabolite of the steroid methyl­oestrenol contains four fused rings A, B, C and D. Ring A adopts a half-chair and the trans-fused rings B and C adopt chair confirmations; the five-membered D ring is folded like an envelope. In the crystal, adjacent mol­ecules are linked by O—H⋯O(carbon­yl) and O—H⋯O(hy­droxy) hydrogen bonds into a layer structure.
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spelling pubmed-30092982010-12-30 17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one Yousuf, Sammer Zafar, Salman Choudhary, Muhammed Iqbal Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(28)O(3), the fungal-transformed metabolite of the steroid methyl­oestrenol contains four fused rings A, B, C and D. Ring A adopts a half-chair and the trans-fused rings B and C adopt chair confirmations; the five-membered D ring is folded like an envelope. In the crystal, adjacent mol­ecules are linked by O—H⋯O(carbon­yl) and O—H⋯O(hy­droxy) hydrogen bonds into a layer structure. International Union of Crystallography 2010-10-23 /pmc/articles/PMC3009298/ /pubmed/21589072 http://dx.doi.org/10.1107/S160053681004033X Text en © Yousuf et al. 2010 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
Yousuf, Sammer
Zafar, Salman
Choudhary, Muhammed Iqbal
Ng, Seik Weng
17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
title 17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
title_full 17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
title_fullStr 17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
title_full_unstemmed 17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
title_short 17β-Hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
title_sort 17β-hy­droxy-17α-(hy­droxy­meth­yl)estr-4-en-3-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009298/
https://www.ncbi.nlm.nih.gov/pubmed/21589072
http://dx.doi.org/10.1107/S160053681004033X
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AT ngseikweng 17bhydroxy17ahydroxymethylestr4en3one

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