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[Sulfonylbis(bromomethylene)]dibenzene
The title compound, C(14)H(12)Br(2)O(2)S, crystallizes as the meso isomer of a diastereoisomeric pair. This structure determination was key to determining that the 1,3 elimination of bromine by triphenylphosphine occurs with inversion of the configuration at each of the two chiral carbon atoms. In...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028549/ https://www.ncbi.nlm.nih.gov/pubmed/36337089 http://dx.doi.org/10.1107/S2414314621013511 |
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author | Corfield, Peter W. R. |
author_facet | Corfield, Peter W. R. |
author_sort | Corfield, Peter W. R. |
collection | PubMed |
description | The title compound, C(14)H(12)Br(2)O(2)S, crystallizes as the meso isomer of a diastereoisomeric pair. This structure determination was key to determining that the 1,3 elimination of bromine by triphenylphosphine occurs with inversion of the configuration at each of the two chiral carbon atoms. In the crystal, the molecules are linked by weak C—H⋯O and C—H⋯Br hydrogen bonds. [Image: see text] |
format | Online Article Text |
id | pubmed-9028549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-90285492022-11-04 [Sulfonylbis(bromomethylene)]dibenzene Corfield, Peter W. R. IUCrdata Data Reports The title compound, C(14)H(12)Br(2)O(2)S, crystallizes as the meso isomer of a diastereoisomeric pair. This structure determination was key to determining that the 1,3 elimination of bromine by triphenylphosphine occurs with inversion of the configuration at each of the two chiral carbon atoms. In the crystal, the molecules are linked by weak C—H⋯O and C—H⋯Br hydrogen bonds. [Image: see text] International Union of Crystallography 2022-01-07 /pmc/articles/PMC9028549/ /pubmed/36337089 http://dx.doi.org/10.1107/S2414314621013511 Text en © Peter W. R. Corfield 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Data Reports Corfield, Peter W. R. [Sulfonylbis(bromomethylene)]dibenzene |
title | [Sulfonylbis(bromomethylene)]dibenzene |
title_full | [Sulfonylbis(bromomethylene)]dibenzene |
title_fullStr | [Sulfonylbis(bromomethylene)]dibenzene |
title_full_unstemmed | [Sulfonylbis(bromomethylene)]dibenzene |
title_short | [Sulfonylbis(bromomethylene)]dibenzene |
title_sort | [sulfonylbis(bromomethylene)]dibenzene |
topic | Data Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028549/ https://www.ncbi.nlm.nih.gov/pubmed/36337089 http://dx.doi.org/10.1107/S2414314621013511 |
work_keys_str_mv | AT corfieldpeterwr sulfonylbisbromomethylenedibenzene |