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(1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate
In the title compound, C(17)H(16)O(7), which was isolated from the leaves of Micromelum integerrimum, the furan ring adopts an envelope conformation with the O atom as the flap. An intramolecular C—H⋯O hydrogen bond occurs. The carbonyl O atom is disordered in a 0.57 (8):0.43 (8) ratio. In the crys...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589005/ https://www.ncbi.nlm.nih.gov/pubmed/23476241 http://dx.doi.org/10.1107/S1600536812047617 |
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author | Phakhodee, Wong Laphookhieo, Surat Prior, Timothy John Rujiwatra, Apinpus |
author_facet | Phakhodee, Wong Laphookhieo, Surat Prior, Timothy John Rujiwatra, Apinpus |
author_sort | Phakhodee, Wong |
collection | PubMed |
description | In the title compound, C(17)H(16)O(7), which was isolated from the leaves of Micromelum integerrimum, the furan ring adopts an envelope conformation with the O atom as the flap. An intramolecular C—H⋯O hydrogen bond occurs. The carbonyl O atom is disordered in a 0.57 (8):0.43 (8) ratio. In the crystal, molecules are linked by weak C—H⋯O hydrogen bonds into a C(10) chain along [010]. |
format | Online Article Text |
id | pubmed-3589005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35890052013-03-08 (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate Phakhodee, Wong Laphookhieo, Surat Prior, Timothy John Rujiwatra, Apinpus Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(16)O(7), which was isolated from the leaves of Micromelum integerrimum, the furan ring adopts an envelope conformation with the O atom as the flap. An intramolecular C—H⋯O hydrogen bond occurs. The carbonyl O atom is disordered in a 0.57 (8):0.43 (8) ratio. In the crystal, molecules are linked by weak C—H⋯O hydrogen bonds into a C(10) chain along [010]. International Union of Crystallography 2012-11-24 /pmc/articles/PMC3589005/ /pubmed/23476241 http://dx.doi.org/10.1107/S1600536812047617 Text en © Phakhodee et al. 2012 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 Phakhodee, Wong Laphookhieo, Surat Prior, Timothy John Rujiwatra, Apinpus (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
title | (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
title_full | (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
title_fullStr | (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
title_full_unstemmed | (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
title_short | (1R,3R,4R,6S)-4-(7-Methoxy-2-oxo-2H-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
title_sort | (1r,3r,4r,6s)-4-(7-methoxy-2-oxo-2h-chromen-6-yl)-1-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl acetate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589005/ https://www.ncbi.nlm.nih.gov/pubmed/23476241 http://dx.doi.org/10.1107/S1600536812047617 |
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