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{(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol

In the title compound, C(37)H(35)NO(3), a precursor to novel chiral catalysts, the N-containing six-membered ring assumes a half-chair conformation. Inter­molecular C—H⋯O hydrogen bonds link the mol­ecules in the crystal structure.

Detalles Bibliográficos
Autores principales: Naicker, Tricia, Govender, Thavendran, Kruger, Hendrik G., Maguire, Glenn E.M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983732/
https://www.ncbi.nlm.nih.gov/pubmed/21580394
http://dx.doi.org/10.1107/S1600536810005295
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author Naicker, Tricia
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E.M.
author_facet Naicker, Tricia
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E.M.
author_sort Naicker, Tricia
collection PubMed
description In the title compound, C(37)H(35)NO(3), a precursor to novel chiral catalysts, the N-containing six-membered ring assumes a half-chair conformation. Inter­molecular C—H⋯O hydrogen bonds link the mol­ecules in the crystal structure.
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spelling pubmed-29837322010-12-30 {(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol Naicker, Tricia Govender, Thavendran Kruger, Hendrik G. Maguire, Glenn E.M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(37)H(35)NO(3), a precursor to novel chiral catalysts, the N-containing six-membered ring assumes a half-chair conformation. Inter­molecular C—H⋯O hydrogen bonds link the mol­ecules in the crystal structure. International Union of Crystallography 2010-02-17 /pmc/articles/PMC2983732/ /pubmed/21580394 http://dx.doi.org/10.1107/S1600536810005295 Text en © Naicker et al. 2010 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
Naicker, Tricia
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E.M.
{(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
title {(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
title_full {(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
title_fullStr {(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
title_full_unstemmed {(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
title_short {(1R,3S)-2-Benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
title_sort {(1r,3s)-2-benzyl-6,7-dimeth­oxy-1-phenyl-1,2,3,4-tetra­hydro­isoquinolin-3-yl}diphenyl­methanol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983732/
https://www.ncbi.nlm.nih.gov/pubmed/21580394
http://dx.doi.org/10.1107/S1600536810005295
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