Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate

The title compound, C(13)H(16)F(6)NO(5)PS, is of inter­est with respect to inhibition of serine hydro­lases. Its structure contains a 1.8797 (13) Å P—C bond and two inter­molecular N—H⋯O=P hydrogen bonds, resulting in centrosymmetric dimers. An intra­molecular N—H⋯O=P hydrogen bond is also present....

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Autores principales: Wijeyesakere, Sanjeeva J., Nasser, Faik A., Kampf, Jeff W., Aksinenko, Alexey Y., Sokolov, Vladimir B., Malygin, Vladimir V., Makhaeva, Galina F., Richardson, Rudy J.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600860/
https://www.ncbi.nlm.nih.gov/pubmed/19079747
http://dx.doi.org/10.1107/S1600536808020175
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author Wijeyesakere, Sanjeeva J.
Nasser, Faik A.
Kampf, Jeff W.
Aksinenko, Alexey Y.
Sokolov, Vladimir B.
Malygin, Vladimir V.
Makhaeva, Galina F.
Richardson, Rudy J.
author_facet Wijeyesakere, Sanjeeva J.
Nasser, Faik A.
Kampf, Jeff W.
Aksinenko, Alexey Y.
Sokolov, Vladimir B.
Malygin, Vladimir V.
Makhaeva, Galina F.
Richardson, Rudy J.
author_sort Wijeyesakere, Sanjeeva J.
collection PubMed
description The title compound, C(13)H(16)F(6)NO(5)PS, is of inter­est with respect to inhibition of serine hydro­lases. Its structure contains a 1.8797 (13) Å P—C bond and two inter­molecular N—H⋯O=P hydrogen bonds, resulting in centrosymmetric dimers. An intra­molecular N—H⋯O=P hydrogen bond is also present.
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spelling pubmed-26008602008-12-11 Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate Wijeyesakere, Sanjeeva J. Nasser, Faik A. Kampf, Jeff W. Aksinenko, Alexey Y. Sokolov, Vladimir B. Malygin, Vladimir V. Makhaeva, Galina F. Richardson, Rudy J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(16)F(6)NO(5)PS, is of inter­est with respect to inhibition of serine hydro­lases. Its structure contains a 1.8797 (13) Å P—C bond and two inter­molecular N—H⋯O=P hydrogen bonds, resulting in centrosymmetric dimers. An intra­molecular N—H⋯O=P hydrogen bond is also present. International Union of Crystallography 2008-07-05 /pmc/articles/PMC2600860/ /pubmed/19079747 http://dx.doi.org/10.1107/S1600536808020175 Text en © Wijeyesakere et al. 2008 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
Wijeyesakere, Sanjeeva J.
Nasser, Faik A.
Kampf, Jeff W.
Aksinenko, Alexey Y.
Sokolov, Vladimir B.
Malygin, Vladimir V.
Makhaeva, Galina F.
Richardson, Rudy J.
Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
title Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
title_full Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
title_fullStr Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
title_full_unstemmed Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
title_short Diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
title_sort diethyl [2,2,2-trifluoro-1-phenyl­sulfonyl­amino-1-(trifluoro­meth­yl)eth­yl]phospho­nate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2600860/
https://www.ncbi.nlm.nih.gov/pubmed/19079747
http://dx.doi.org/10.1107/S1600536808020175
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