2,6-Anhydro-1,3-di-O-benzyl-d-mannitol

In the title compound, C(20)H(24)O(5), the six-membered pyran­ose ring adopts a chair conformation. The dihedral angle between the planes of the phenyl groups of the benzyl substituents is 63.1°. Two types of inter­molecular O—H⋯O hydrogen bonds lead to the formation of infinite chains along the b a...

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Detalles Bibliográficos
Autores principales: de Siqueira, Edmilson Clarindo, Doboszewski, Bogdan, McGarrah, James, Nazarenko, Alexander Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152021/
https://www.ncbi.nlm.nih.gov/pubmed/21837055
http://dx.doi.org/10.1107/S1600536811022306
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author de Siqueira, Edmilson Clarindo
Doboszewski, Bogdan
McGarrah, James
Nazarenko, Alexander Y.
author_facet de Siqueira, Edmilson Clarindo
Doboszewski, Bogdan
McGarrah, James
Nazarenko, Alexander Y.
author_sort de Siqueira, Edmilson Clarindo
collection PubMed
description In the title compound, C(20)H(24)O(5), the six-membered pyran­ose ring adopts a chair conformation. The dihedral angle between the planes of the phenyl groups of the benzyl substituents is 63.1°. Two types of inter­molecular O—H⋯O hydrogen bonds lead to the formation of infinite chains along the b axis. Only weak C—H⋯O contacts exist between neighboring chains.
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spelling pubmed-31520212011-08-11 2,6-Anhydro-1,3-di-O-benzyl-d-mannitol de Siqueira, Edmilson Clarindo Doboszewski, Bogdan McGarrah, James Nazarenko, Alexander Y. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(24)O(5), the six-membered pyran­ose ring adopts a chair conformation. The dihedral angle between the planes of the phenyl groups of the benzyl substituents is 63.1°. Two types of inter­molecular O—H⋯O hydrogen bonds lead to the formation of infinite chains along the b axis. Only weak C—H⋯O contacts exist between neighboring chains. International Union of Crystallography 2011-06-18 /pmc/articles/PMC3152021/ /pubmed/21837055 http://dx.doi.org/10.1107/S1600536811022306 Text en © Siqueira et al. 2011 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
de Siqueira, Edmilson Clarindo
Doboszewski, Bogdan
McGarrah, James
Nazarenko, Alexander Y.
2,6-Anhydro-1,3-di-O-benzyl-d-mannitol
title 2,6-Anhydro-1,3-di-O-benzyl-d-mannitol
title_full 2,6-Anhydro-1,3-di-O-benzyl-d-mannitol
title_fullStr 2,6-Anhydro-1,3-di-O-benzyl-d-mannitol
title_full_unstemmed 2,6-Anhydro-1,3-di-O-benzyl-d-mannitol
title_short 2,6-Anhydro-1,3-di-O-benzyl-d-mannitol
title_sort 2,6-anhydro-1,3-di-o-benzyl-d-mannitol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152021/
https://www.ncbi.nlm.nih.gov/pubmed/21837055
http://dx.doi.org/10.1107/S1600536811022306
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AT doboszewskibogdan 26anhydro13diobenzyldmannitol
AT mcgarrahjames 26anhydro13diobenzyldmannitol
AT nazarenkoalexandery 26anhydro13diobenzyldmannitol

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