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2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide

The title compound, C(5)H(9)O(4)PS, was synthesized by the reaction of penta­erythritol with thio­phosphoryl chloride. In the crystal structure, the three six-membered rings all adopt boat conformations. Mol­ecules form chains along the c axis via inter­molecular O—H⋯O hydrogen bonds.

Detalles Bibliográficos
Autores principales: Yang, Qi, Zhang, Ye-qin, Huang, Jian-qian, Men, Jian, Gao, Guo-wei
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968057/
https://www.ncbi.nlm.nih.gov/pubmed/21581600
http://dx.doi.org/10.1107/S1600536808041937
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author Yang, Qi
Zhang, Ye-qin
Huang, Jian-qian
Men, Jian
Gao, Guo-wei
author_facet Yang, Qi
Zhang, Ye-qin
Huang, Jian-qian
Men, Jian
Gao, Guo-wei
author_sort Yang, Qi
collection PubMed
description The title compound, C(5)H(9)O(4)PS, was synthesized by the reaction of penta­erythritol with thio­phosphoryl chloride. In the crystal structure, the three six-membered rings all adopt boat conformations. Mol­ecules form chains along the c axis via inter­molecular O—H⋯O hydrogen bonds.
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spelling pubmed-29680572010-12-30 2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide Yang, Qi Zhang, Ye-qin Huang, Jian-qian Men, Jian Gao, Guo-wei Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(5)H(9)O(4)PS, was synthesized by the reaction of penta­erythritol with thio­phosphoryl chloride. In the crystal structure, the three six-membered rings all adopt boat conformations. Mol­ecules form chains along the c axis via inter­molecular O—H⋯O hydrogen bonds. International Union of Crystallography 2008-12-17 /pmc/articles/PMC2968057/ /pubmed/21581600 http://dx.doi.org/10.1107/S1600536808041937 Text en © Yang et al. 2009 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
Yang, Qi
Zhang, Ye-qin
Huang, Jian-qian
Men, Jian
Gao, Guo-wei
2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
title 2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
title_full 2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
title_fullStr 2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
title_full_unstemmed 2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
title_short 2,6,7-Trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
title_sort 2,6,7-trioxa-1-phosphabicyclo­[2.2.2]octan-4-ylmethanol 1-sulfide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968057/
https://www.ncbi.nlm.nih.gov/pubmed/21581600
http://dx.doi.org/10.1107/S1600536808041937
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