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5α-Androst-3-en-17β-yl acetate
In the crystal structure of the title compound, C(21)H(32)O(2), ring A is highly distorted, with a conformation intermediate between 10β-sofa and 1α,10β-half chair; rings B and C have slightly flattened chair conformations. Ring D assumes an unusual 13β-envelope conformation, probably induced by th...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979999/ https://www.ncbi.nlm.nih.gov/pubmed/21580068 http://dx.doi.org/10.1107/S1600536809053264 |
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author | Andrade, L. C. R. Paixão, J. A. de Almeida, M. J. M. Tavares da Silva, E. J. Fernandes Roleira, F. M. |
author_facet | Andrade, L. C. R. Paixão, J. A. de Almeida, M. J. M. Tavares da Silva, E. J. Fernandes Roleira, F. M. |
author_sort | Andrade, L. C. R. |
collection | PubMed |
description | In the crystal structure of the title compound, C(21)H(32)O(2), ring A is highly distorted, with a conformation intermediate between 10β-sofa and 1α,10β-half chair; rings B and C have slightly flattened chair conformations. Ring D assumes an unusual 13β-envelope conformation, probably induced by the acetoxy substituent. Cohesion of the crystal structure is due only to weak van der Waals interactions. |
format | Text |
id | pubmed-2979999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29799992010-12-30 5α-Androst-3-en-17β-yl acetate Andrade, L. C. R. Paixão, J. A. de Almeida, M. J. M. Tavares da Silva, E. J. Fernandes Roleira, F. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(21)H(32)O(2), ring A is highly distorted, with a conformation intermediate between 10β-sofa and 1α,10β-half chair; rings B and C have slightly flattened chair conformations. Ring D assumes an unusual 13β-envelope conformation, probably induced by the acetoxy substituent. Cohesion of the crystal structure is due only to weak van der Waals interactions. International Union of Crystallography 2009-12-16 /pmc/articles/PMC2979999/ /pubmed/21580068 http://dx.doi.org/10.1107/S1600536809053264 Text en © Andrade 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 Andrade, L. C. R. Paixão, J. A. de Almeida, M. J. M. Tavares da Silva, E. J. Fernandes Roleira, F. M. 5α-Androst-3-en-17β-yl acetate |
title | 5α-Androst-3-en-17β-yl acetate |
title_full | 5α-Androst-3-en-17β-yl acetate |
title_fullStr | 5α-Androst-3-en-17β-yl acetate |
title_full_unstemmed | 5α-Androst-3-en-17β-yl acetate |
title_short | 5α-Androst-3-en-17β-yl acetate |
title_sort | 5α-androst-3-en-17β-yl acetate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979999/ https://www.ncbi.nlm.nih.gov/pubmed/21580068 http://dx.doi.org/10.1107/S1600536809053264 |
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