4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate

The absolute configuration of the title compound, C(12)H(15)NO(7)·0.5H(2)O, was assigned from the synthesis. There are two rhamnoside mol­ecules and one water mol­ecule in the asymmetric unit, displaying O—H⋯O hydrogen bonding. One of the nitro groups does not conjugate efficiently with the benzene...

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Detalles Bibliográficos
Autores principales: Zhang, Jianbo, Fu, Jie, Chen, Xuan, Gu, Yijun, Tang, Jie
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960897/
https://www.ncbi.nlm.nih.gov/pubmed/21202105
http://dx.doi.org/10.1107/S1600536808006387
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author Zhang, Jianbo
Fu, Jie
Chen, Xuan
Gu, Yijun
Tang, Jie
author_facet Zhang, Jianbo
Fu, Jie
Chen, Xuan
Gu, Yijun
Tang, Jie
author_sort Zhang, Jianbo
collection PubMed
description The absolute configuration of the title compound, C(12)H(15)NO(7)·0.5H(2)O, was assigned from the synthesis. There are two rhamnoside mol­ecules and one water mol­ecule in the asymmetric unit, displaying O—H⋯O hydrogen bonding. One of the nitro groups does not conjugate efficiently with the benzene ring.
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spelling pubmed-29608972010-12-30 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate Zhang, Jianbo Fu, Jie Chen, Xuan Gu, Yijun Tang, Jie Acta Crystallogr Sect E Struct Rep Online Organic Papers The absolute configuration of the title compound, C(12)H(15)NO(7)·0.5H(2)O, was assigned from the synthesis. There are two rhamnoside mol­ecules and one water mol­ecule in the asymmetric unit, displaying O—H⋯O hydrogen bonding. One of the nitro groups does not conjugate efficiently with the benzene ring. International Union of Crystallography 2008-03-14 /pmc/articles/PMC2960897/ /pubmed/21202105 http://dx.doi.org/10.1107/S1600536808006387 Text en © Zhang 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
Zhang, Jianbo
Fu, Jie
Chen, Xuan
Gu, Yijun
Tang, Jie
4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_full 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_fullStr 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_full_unstemmed 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_short 4-Nitro­phenyl α-l-rhamnopyran­oside hemihydrate
title_sort 4-nitro­phenyl α-l-rhamnopyran­oside hemihydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960897/
https://www.ncbi.nlm.nih.gov/pubmed/21202105
http://dx.doi.org/10.1107/S1600536808006387
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AT fujie 4nitrophenylalrhamnopyranosidehemihydrate
AT chenxuan 4nitrophenylalrhamnopyranosidehemihydrate
AT guyijun 4nitrophenylalrhamnopyranosidehemihydrate
AT tangjie 4nitrophenylalrhamnopyranosidehemihydrate

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