(R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide

The title compound, C(14)H(30)N(2)O(2)S(2), is the product of the monoaddition reaction of tert-butyl magnesium chloride with bis-[(R)-N-tert-butanesulfinyl]ethanediimine. There are two almost identical mol­ecules in the asymmetric unit, the mol­ecular conformation of which is stabilized by an intra...

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Detalles Bibliográficos
Autores principales: Hu, Yu, Sun, Xiao-Xia, Fan, Cong-Bin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959383/
https://www.ncbi.nlm.nih.gov/pubmed/21201122
http://dx.doi.org/10.1107/S1600536808028225
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author Hu, Yu
Sun, Xiao-Xia
Fan, Cong-Bin
author_facet Hu, Yu
Sun, Xiao-Xia
Fan, Cong-Bin
author_sort Hu, Yu
collection PubMed
description The title compound, C(14)H(30)N(2)O(2)S(2), is the product of the monoaddition reaction of tert-butyl magnesium chloride with bis-[(R)-N-tert-butanesulfinyl]ethanediimine. There are two almost identical mol­ecules in the asymmetric unit, the mol­ecular conformation of which is stabilized by an intra­molecular N—H⋯N hydrogen bond.
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spelling pubmed-29593832010-12-30 (R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide Hu, Yu Sun, Xiao-Xia Fan, Cong-Bin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(30)N(2)O(2)S(2), is the product of the monoaddition reaction of tert-butyl magnesium chloride with bis-[(R)-N-tert-butanesulfinyl]ethanediimine. There are two almost identical mol­ecules in the asymmetric unit, the mol­ecular conformation of which is stabilized by an intra­molecular N—H⋯N hydrogen bond. International Union of Crystallography 2008-09-13 /pmc/articles/PMC2959383/ /pubmed/21201122 http://dx.doi.org/10.1107/S1600536808028225 Text en © Hu 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
Hu, Yu
Sun, Xiao-Xia
Fan, Cong-Bin
(R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
title (R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
title_full (R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
title_fullStr (R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
title_full_unstemmed (R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
title_short (R)-N-{2-tert-Butyl-2-[(R)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
title_sort (r)-n-{2-tert-butyl-2-[(r)-tert-butyl­sulfonamido]ethylidene}-tert-butane­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959383/
https://www.ncbi.nlm.nih.gov/pubmed/21201122
http://dx.doi.org/10.1107/S1600536808028225
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AT sunxiaoxia rn2tertbutyl2rtertbutylsulfonamidoethylidenetertbutanesulfonamide
AT fancongbin rn2tertbutyl2rtertbutylsulfonamidoethylidenetertbutanesulfonamide

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