1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan

In the title compound, C(19)H(20)O(2)S, the cyclo­hexyl ring adopts a chair conformation and the aryl­sulfinyl unit is positioned equatorial relative to the cyclo­hexyl group. In the crystal, mol­ecules are linked through weak inter­molecular C—H⋯O hydrogen bonds. The O atom of the sulfinyl group is...

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Detalles Bibliográficos
Autores principales: Choi, Hong Dae, Seo, Pil Ja, Son, Byeng Wha, Lee, Uk
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100045/
https://www.ncbi.nlm.nih.gov/pubmed/21754023
http://dx.doi.org/10.1107/S1600536811010981
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author Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
author_facet Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
author_sort Choi, Hong Dae
collection PubMed
description In the title compound, C(19)H(20)O(2)S, the cyclo­hexyl ring adopts a chair conformation and the aryl­sulfinyl unit is positioned equatorial relative to the cyclo­hexyl group. In the crystal, mol­ecules are linked through weak inter­molecular C—H⋯O hydrogen bonds. The O atom of the sulfinyl group is disordered over two orientations with site-occupancy factors of 0.923 (3) and 0.077 (3).
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spelling pubmed-31000452011-07-13 1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(20)O(2)S, the cyclo­hexyl ring adopts a chair conformation and the aryl­sulfinyl unit is positioned equatorial relative to the cyclo­hexyl group. In the crystal, mol­ecules are linked through weak inter­molecular C—H⋯O hydrogen bonds. The O atom of the sulfinyl group is disordered over two orientations with site-occupancy factors of 0.923 (3) and 0.077 (3). International Union of Crystallography 2011-03-31 /pmc/articles/PMC3100045/ /pubmed/21754023 http://dx.doi.org/10.1107/S1600536811010981 Text en © Choi 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
Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
title 1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
title_full 1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
title_fullStr 1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
title_full_unstemmed 1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
title_short 1-Cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
title_sort 1-cyclo­hexyl­sulfinyl-2-methyl­naphtho­[2,1-b]furan
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100045/
https://www.ncbi.nlm.nih.gov/pubmed/21754023
http://dx.doi.org/10.1107/S1600536811010981
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AT leeuk 1cyclohexylsulfinyl2methylnaphtho21bfuran

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