(S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate

The title compound, C(35)H(31)NO(3), was obtained by the reaction of (S)-benzyl 2-amino-3-(4-hy­droxy­phen­yl)propano­ate and (chloro­methane­tri­yl)tribenzene. The enanti­omer has been assigned by reference to an unchanging chiral centre in the synthetic procedure. In the crystal, mol­ecules are li...

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Detalles Bibliográficos
Autores principales: Chen, Meimei, Lai, Xinmei, Zhou, Changen, Yang, Xuemei
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/PMC3120518/
https://www.ncbi.nlm.nih.gov/pubmed/21754794
http://dx.doi.org/10.1107/S1600536811017351
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author Chen, Meimei
Lai, Xinmei
Zhou, Changen
Yang, Xuemei
author_facet Chen, Meimei
Lai, Xinmei
Zhou, Changen
Yang, Xuemei
author_sort Chen, Meimei
collection PubMed
description The title compound, C(35)H(31)NO(3), was obtained by the reaction of (S)-benzyl 2-amino-3-(4-hy­droxy­phen­yl)propano­ate and (chloro­methane­tri­yl)tribenzene. The enanti­omer has been assigned by reference to an unchanging chiral centre in the synthetic procedure. In the crystal, mol­ecules are linked into chains running along the a axis by inter­molecular O—H⋯O hydrogen bonds.
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spelling pubmed-31205182011-07-13 (S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate Chen, Meimei Lai, Xinmei Zhou, Changen Yang, Xuemei Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(35)H(31)NO(3), was obtained by the reaction of (S)-benzyl 2-amino-3-(4-hy­droxy­phen­yl)propano­ate and (chloro­methane­tri­yl)tribenzene. The enanti­omer has been assigned by reference to an unchanging chiral centre in the synthetic procedure. In the crystal, mol­ecules are linked into chains running along the a axis by inter­molecular O—H⋯O hydrogen bonds. International Union of Crystallography 2011-05-14 /pmc/articles/PMC3120518/ /pubmed/21754794 http://dx.doi.org/10.1107/S1600536811017351 Text en © Chen 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
Chen, Meimei
Lai, Xinmei
Zhou, Changen
Yang, Xuemei
(S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
title (S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
title_full (S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
title_fullStr (S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
title_full_unstemmed (S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
title_short (S)-Benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
title_sort (s)-benzyl 3-(4-hy­droxy­phen­yl)-2-(trityl­amino)­propano­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120518/
https://www.ncbi.nlm.nih.gov/pubmed/21754794
http://dx.doi.org/10.1107/S1600536811017351
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