N-Trityl-2-(tritylsulfan­yl)aniline

The title compound, C(44)H(35)NS, is a derivative of amino­thio­phenol and possesses a protected S-triphenyl­methyl thio­ether and an N-triphenyl­methyl­amine functional group. The trityl groups show an anti orientation, with C—C—N—C and C—C—S—C torsion angles of −151.0 (3) and −105.3 (2)°, respecti...

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Detalles Bibliográficos
Autores principales: Neuba, Adam, Flörke, Ulrich, Henkel, Gerald
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/PMC3247617/
https://www.ncbi.nlm.nih.gov/pubmed/22219922
http://dx.doi.org/10.1107/S1600536811039183
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author Neuba, Adam
Flörke, Ulrich
Henkel, Gerald
author_facet Neuba, Adam
Flörke, Ulrich
Henkel, Gerald
author_sort Neuba, Adam
collection PubMed
description The title compound, C(44)H(35)NS, is a derivative of amino­thio­phenol and possesses a protected S-triphenyl­methyl thio­ether and an N-triphenyl­methyl­amine functional group. The trityl groups show an anti orientation, with C—C—N—C and C—C—S—C torsion angles of −151.0 (3) and −105.3 (2)°, respectively. There is an intra­molecular N—H⋯S hydrogen bond.
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spelling pubmed-32476172012-01-04 N-Trityl-2-(tritylsulfan­yl)aniline Neuba, Adam Flörke, Ulrich Henkel, Gerald Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(44)H(35)NS, is a derivative of amino­thio­phenol and possesses a protected S-triphenyl­methyl thio­ether and an N-triphenyl­methyl­amine functional group. The trityl groups show an anti orientation, with C—C—N—C and C—C—S—C torsion angles of −151.0 (3) and −105.3 (2)°, respectively. There is an intra­molecular N—H⋯S hydrogen bond. International Union of Crystallography 2011-10-08 /pmc/articles/PMC3247617/ /pubmed/22219922 http://dx.doi.org/10.1107/S1600536811039183 Text en © Neuba 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
Neuba, Adam
Flörke, Ulrich
Henkel, Gerald
N-Trityl-2-(tritylsulfan­yl)aniline
title N-Trityl-2-(tritylsulfan­yl)aniline
title_full N-Trityl-2-(tritylsulfan­yl)aniline
title_fullStr N-Trityl-2-(tritylsulfan­yl)aniline
title_full_unstemmed N-Trityl-2-(tritylsulfan­yl)aniline
title_short N-Trityl-2-(tritylsulfan­yl)aniline
title_sort n-trityl-2-(tritylsulfan­yl)aniline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247617/
https://www.ncbi.nlm.nih.gov/pubmed/22219922
http://dx.doi.org/10.1107/S1600536811039183
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