tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate

The relative stereochemistry of the title compound, C(20)H(23)NO(3), was established by X-ray analysis. The asymmetric unit contains two independent mol­ecules. In the crystal structure, each type of mol­ecule forms a centrosymmetric dimer via pairs of inter­molecular O—H⋯O hydrogen bonds, resulting...

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Detalles Bibliográficos
Autores principales: Lough, Alan J., Machin, Ben P., Tam, William
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969270/
https://www.ncbi.nlm.nih.gov/pubmed/21582783
http://dx.doi.org/10.1107/S1600536809020315
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author Lough, Alan J.
Machin, Ben P.
Tam, William
author_facet Lough, Alan J.
Machin, Ben P.
Tam, William
author_sort Lough, Alan J.
collection PubMed
description The relative stereochemistry of the title compound, C(20)H(23)NO(3), was established by X-ray analysis. The asymmetric unit contains two independent mol­ecules. In the crystal structure, each type of mol­ecule forms a centrosymmetric dimer via pairs of inter­molecular O—H⋯O hydrogen bonds, resulting in an R (2) (2)(10) loop in each case.
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spelling pubmed-29692702010-12-30 tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate Lough, Alan J. Machin, Ben P. Tam, William Acta Crystallogr Sect E Struct Rep Online Organic Papers The relative stereochemistry of the title compound, C(20)H(23)NO(3), was established by X-ray analysis. The asymmetric unit contains two independent mol­ecules. In the crystal structure, each type of mol­ecule forms a centrosymmetric dimer via pairs of inter­molecular O—H⋯O hydrogen bonds, resulting in an R (2) (2)(10) loop in each case. International Union of Crystallography 2009-06-06 /pmc/articles/PMC2969270/ /pubmed/21582783 http://dx.doi.org/10.1107/S1600536809020315 Text en © Lough et al. 2009 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
Lough, Alan J.
Machin, Ben P.
Tam, William
tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
title tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
title_full tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
title_fullStr tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
title_full_unstemmed tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
title_short tert-Butyl N-hydr­oxy-N-[(1S*,2R*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
title_sort tert-butyl n-hydr­oxy-n-[(1s*,2r*)-2-(1-naphth­yl)cyclo­pent-3-en-1-yl]carbamate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969270/
https://www.ncbi.nlm.nih.gov/pubmed/21582783
http://dx.doi.org/10.1107/S1600536809020315
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AT machinbenp tertbutylnhydroxyn1s2r21naphthylcyclopent3en1ylcarbamate
AT tamwilliam tertbutylnhydroxyn1s2r21naphthylcyclopent3en1ylcarbamate

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