Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate

The heterocyclic core of the title compound, C(10)H(17)NO(5), adopts a chair conformation with its three C substituents positioned equatorially. In the crystal, inter­molecular O—H⋯N hydrogen bonds between neighbouring mol­ecules lead to chains along b. These chains are connected by hydro­phobic int...

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Detalles Bibliográficos
Autores principales: Hartung, Jens, Stapf, Georg, Bergsträsser, Uwe
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979220/
https://www.ncbi.nlm.nih.gov/pubmed/21579077
http://dx.doi.org/10.1107/S1600536810010925
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author Hartung, Jens
Stapf, Georg
Bergsträsser, Uwe
author_facet Hartung, Jens
Stapf, Georg
Bergsträsser, Uwe
author_sort Hartung, Jens
collection PubMed
description The heterocyclic core of the title compound, C(10)H(17)NO(5), adopts a chair conformation with its three C substituents positioned equatorially. In the crystal, inter­molecular O—H⋯N hydrogen bonds between neighbouring mol­ecules lead to chains along b. These chains are connected by hydro­phobic inter­actions, forming infinite layers and N—H⋯O=C contacts between mol­ecules of adjacent layers give rise to a three-dimensional structure.
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spelling pubmed-29792202010-12-30 Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate Hartung, Jens Stapf, Georg Bergsträsser, Uwe Acta Crystallogr Sect E Struct Rep Online Organic Papers The heterocyclic core of the title compound, C(10)H(17)NO(5), adopts a chair conformation with its three C substituents positioned equatorially. In the crystal, inter­molecular O—H⋯N hydrogen bonds between neighbouring mol­ecules lead to chains along b. These chains are connected by hydro­phobic inter­actions, forming infinite layers and N—H⋯O=C contacts between mol­ecules of adjacent layers give rise to a three-dimensional structure. International Union of Crystallography 2010-04-02 /pmc/articles/PMC2979220/ /pubmed/21579077 http://dx.doi.org/10.1107/S1600536810010925 Text en © Hartung 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
Hartung, Jens
Stapf, Georg
Bergsträsser, Uwe
Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
title Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
title_full Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
title_fullStr Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
title_full_unstemmed Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
title_short Dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
title_sort dimethyl cis-4-hydroxy­methyl­piperidine-2,6-dicarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979220/
https://www.ncbi.nlm.nih.gov/pubmed/21579077
http://dx.doi.org/10.1107/S1600536810010925
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AT stapfgeorg dimethylcis4hydroxymethylpiperidine26dicarboxylate
AT bergstrasseruwe dimethylcis4hydroxymethylpiperidine26dicarboxylate

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