N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine

The title compound, C(14)H(19)NO(6), was synthesized by the condensation reaction between hecilid (4-formyl­phenl-β-d-allopyran­oside) and methyl­amine in methanol. In the crystal structure, the pyran ring adopts a chair conformation and adjacent mol­ecules are linked by inter­molecular O—H⋯O and O—...

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Detalles Bibliográficos
Autores principales: Lv, Shi-Ming, Zheng, Lei, Zhao, Hui, Li, Ying, Yin, Shu-Fan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968321/
https://www.ncbi.nlm.nih.gov/pubmed/21581901
http://dx.doi.org/10.1107/S1600536809000944
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author Lv, Shi-Ming
Zheng, Lei
Zhao, Hui
Li, Ying
Yin, Shu-Fan
author_facet Lv, Shi-Ming
Zheng, Lei
Zhao, Hui
Li, Ying
Yin, Shu-Fan
author_sort Lv, Shi-Ming
collection PubMed
description The title compound, C(14)H(19)NO(6), was synthesized by the condensation reaction between hecilid (4-formyl­phenl-β-d-allopyran­oside) and methyl­amine in methanol. In the crystal structure, the pyran ring adopts a chair conformation and adjacent mol­ecules are linked by inter­molecular O—H⋯O and O—H⋯N hydrogen bonds, forming a three-dimensional network.
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spelling pubmed-29683212010-12-30 N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine Lv, Shi-Ming Zheng, Lei Zhao, Hui Li, Ying Yin, Shu-Fan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(19)NO(6), was synthesized by the condensation reaction between hecilid (4-formyl­phenl-β-d-allopyran­oside) and methyl­amine in methanol. In the crystal structure, the pyran ring adopts a chair conformation and adjacent mol­ecules are linked by inter­molecular O—H⋯O and O—H⋯N hydrogen bonds, forming a three-dimensional network. International Union of Crystallography 2009-01-10 /pmc/articles/PMC2968321/ /pubmed/21581901 http://dx.doi.org/10.1107/S1600536809000944 Text en © Lv 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
Lv, Shi-Ming
Zheng, Lei
Zhao, Hui
Li, Ying
Yin, Shu-Fan
N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine
title N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine
title_full N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine
title_fullStr N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine
title_full_unstemmed N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine
title_short N-[4-(β-d-Allopyranos­yloxy)benzyl­idene]methyl­amine
title_sort n-[4-(β-d-allopyranos­yloxy)benzyl­idene]methyl­amine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968321/
https://www.ncbi.nlm.nih.gov/pubmed/21581901
http://dx.doi.org/10.1107/S1600536809000944
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AT zhaohui n4bdallopyranosyloxybenzylidenemethylamine
AT liying n4bdallopyranosyloxybenzylidenemethylamine
AT yinshufan n4bdallopyranosyloxybenzylidenemethylamine

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