3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol

The title compound, C(18)H(33)NO(3), was prepared according to a highly diastereoselective hydrogenation procedure from 3,5,7-triallyl-1-aza­adamantane-4,6,10-trione. The crystal structure of the title compound contains two crystallographically independent mol­ecules (Z′ = 2), which are linked by in...

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Detalles Bibliográficos
Autores principales: Saaidi, Pierre-Loïc, Chazal, Pierre-Etienne, Maurin, Philippe, Jeanneau, Erwann, Hasserodt, Jens
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961298/
https://www.ncbi.nlm.nih.gov/pubmed/21202295
http://dx.doi.org/10.1107/S1600536808006284
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author Saaidi, Pierre-Loïc
Chazal, Pierre-Etienne
Maurin, Philippe
Jeanneau, Erwann
Hasserodt, Jens
author_facet Saaidi, Pierre-Loïc
Chazal, Pierre-Etienne
Maurin, Philippe
Jeanneau, Erwann
Hasserodt, Jens
author_sort Saaidi, Pierre-Loïc
collection PubMed
description The title compound, C(18)H(33)NO(3), was prepared according to a highly diastereoselective hydrogenation procedure from 3,5,7-triallyl-1-aza­adamantane-4,6,10-trione. The crystal structure of the title compound contains two crystallographically independent mol­ecules (Z′ = 2), which are linked by inter­molecular hydrogen bonding into chains. In contrast to the aza­adamantanones, the aza­adamantanetriol core of the title compound does not show any particular C—C bond elongation.
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spelling pubmed-29612982010-12-30 3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol Saaidi, Pierre-Loïc Chazal, Pierre-Etienne Maurin, Philippe Jeanneau, Erwann Hasserodt, Jens Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(33)NO(3), was prepared according to a highly diastereoselective hydrogenation procedure from 3,5,7-triallyl-1-aza­adamantane-4,6,10-trione. The crystal structure of the title compound contains two crystallographically independent mol­ecules (Z′ = 2), which are linked by inter­molecular hydrogen bonding into chains. In contrast to the aza­adamantanones, the aza­adamantanetriol core of the title compound does not show any particular C—C bond elongation. International Union of Crystallography 2008-04-04 /pmc/articles/PMC2961298/ /pubmed/21202295 http://dx.doi.org/10.1107/S1600536808006284 Text en © Saaidi 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
Saaidi, Pierre-Loïc
Chazal, Pierre-Etienne
Maurin, Philippe
Jeanneau, Erwann
Hasserodt, Jens
3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol
title 3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol
title_full 3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol
title_fullStr 3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol
title_full_unstemmed 3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol
title_short 3,5,7-Tripropyl-1-aza­adamantane-4,6,10-triol
title_sort 3,5,7-tripropyl-1-aza­adamantane-4,6,10-triol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961298/
https://www.ncbi.nlm.nih.gov/pubmed/21202295
http://dx.doi.org/10.1107/S1600536808006284
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