Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate

In the title compound, C(16)H(23)NO(5), the H—N—O—C torsion angle is 98.6 (1)°, which is of a similar magnitude to other N,O-diacyl­hydroxy­lamines. The N—O distance is 1.4029 (14) Å, which is similar to the N—O distance in other N,O-diacyl­hydroxy­lamines. In the crystal, intermolecular N—H⋯O hydro...

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Detalles Bibliográficos
Autores principales: Liu, Joe, Clegg, Jack K., Codd, Rachel
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977356/
https://www.ncbi.nlm.nih.gov/pubmed/21583454
http://dx.doi.org/10.1107/S1600536809024210
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author Liu, Joe
Clegg, Jack K.
Codd, Rachel
author_facet Liu, Joe
Clegg, Jack K.
Codd, Rachel
author_sort Liu, Joe
collection PubMed
description In the title compound, C(16)H(23)NO(5), the H—N—O—C torsion angle is 98.6 (1)°, which is of a similar magnitude to other N,O-diacyl­hydroxy­lamines. The N—O distance is 1.4029 (14) Å, which is similar to the N—O distance in other N,O-diacyl­hydroxy­lamines. In the crystal, intermolecular N—H⋯O hydrogen bonds generate chains of molecules.
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spelling pubmed-29773562010-12-30 Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate Liu, Joe Clegg, Jack K. Codd, Rachel Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(23)NO(5), the H—N—O—C torsion angle is 98.6 (1)°, which is of a similar magnitude to other N,O-diacyl­hydroxy­lamines. The N—O distance is 1.4029 (14) Å, which is similar to the N—O distance in other N,O-diacyl­hydroxy­lamines. In the crystal, intermolecular N—H⋯O hydrogen bonds generate chains of molecules. International Union of Crystallography 2009-07-04 /pmc/articles/PMC2977356/ /pubmed/21583454 http://dx.doi.org/10.1107/S1600536809024210 Text en © Liu 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
Liu, Joe
Clegg, Jack K.
Codd, Rachel
Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
title Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
title_full Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
title_fullStr Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
title_full_unstemmed Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
title_short Methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
title_sort methyl 3-[(1-adamantylcarbon­yloxy)amino­carbon­yl]propanoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977356/
https://www.ncbi.nlm.nih.gov/pubmed/21583454
http://dx.doi.org/10.1107/S1600536809024210
work_keys_str_mv AT liujoe methyl31adamantylcarbonyloxyaminocarbonylpropanoate
AT cleggjackk methyl31adamantylcarbonyloxyaminocarbonylpropanoate
AT coddrachel methyl31adamantylcarbonyloxyaminocarbonylpropanoate

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