Cholest-5-ene

The asymmetric unit of the title compound, C(27)H(46), contains two crytallographically independent cholest-5-ene mol­ecules (A and B). In each mol­ecule, the three six-membered rings are all in chair conformations, while the five-membered ring is in a twist conformation. The terminal isopropyl grou...

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Autores principales: Khan, Mohd Shaheen, Sulaiman, Othman, Hashim, Rokiah, Hemamalini, Madhukar, Fun, Hoong-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120455/
https://www.ncbi.nlm.nih.gov/pubmed/21754760
http://dx.doi.org/10.1107/S1600536811016783
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author Khan, Mohd Shaheen
Sulaiman, Othman
Hashim, Rokiah
Hemamalini, Madhukar
Fun, Hoong-Kun
author_facet Khan, Mohd Shaheen
Sulaiman, Othman
Hashim, Rokiah
Hemamalini, Madhukar
Fun, Hoong-Kun
author_sort Khan, Mohd Shaheen
collection PubMed
description The asymmetric unit of the title compound, C(27)H(46), contains two crytallographically independent cholest-5-ene mol­ecules (A and B). In each mol­ecule, the three six-membered rings are all in chair conformations, while the five-membered ring is in a twist conformation. The terminal isopropyl group of mol­ecule A has a (−)-gauche conformation, whereas that of mol­ecule B has a (+)-gauche conformation. No significant inter­molecular inter­actions are observed in the crystal structure.
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spelling pubmed-31204552011-07-13 Cholest-5-ene Khan, Mohd Shaheen Sulaiman, Othman Hashim, Rokiah Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(27)H(46), contains two crytallographically independent cholest-5-ene mol­ecules (A and B). In each mol­ecule, the three six-membered rings are all in chair conformations, while the five-membered ring is in a twist conformation. The terminal isopropyl group of mol­ecule A has a (−)-gauche conformation, whereas that of mol­ecule B has a (+)-gauche conformation. No significant inter­molecular inter­actions are observed in the crystal structure. International Union of Crystallography 2011-05-11 /pmc/articles/PMC3120455/ /pubmed/21754760 http://dx.doi.org/10.1107/S1600536811016783 Text en © Khan 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
Khan, Mohd Shaheen
Sulaiman, Othman
Hashim, Rokiah
Hemamalini, Madhukar
Fun, Hoong-Kun
Cholest-5-ene
title Cholest-5-ene
title_full Cholest-5-ene
title_fullStr Cholest-5-ene
title_full_unstemmed Cholest-5-ene
title_short Cholest-5-ene
title_sort cholest-5-ene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120455/
https://www.ncbi.nlm.nih.gov/pubmed/21754760
http://dx.doi.org/10.1107/S1600536811016783
work_keys_str_mv AT khanmohdshaheen cholest5ene
AT sulaimanothman cholest5ene
AT hashimrokiah cholest5ene
AT hemamalinimadhukar cholest5ene
AT funhoongkun cholest5ene

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