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tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate
In the title compound, C(21)H(18)O(6), a previously unknown coumarin derivative, the benzoyl substitutent makes a dihedral angle of 53.80 (16)° with the plane of the coumarin rings. An intramolecular O—H⋯O hydrogen bond is observed.
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961751/ https://www.ncbi.nlm.nih.gov/pubmed/21202843 http://dx.doi.org/10.1107/S1600536808016188 |
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author | Baharfar, Robabeh Vahdat, S. Mohammad Baghbanian, S. Meysam |
author_facet | Baharfar, Robabeh Vahdat, S. Mohammad Baghbanian, S. Meysam |
author_sort | Baharfar, Robabeh |
collection | PubMed |
description | In the title compound, C(21)H(18)O(6), a previously unknown coumarin derivative, the benzoyl substitutent makes a dihedral angle of 53.80 (16)° with the plane of the coumarin rings. An intramolecular O—H⋯O hydrogen bond is observed. |
format | Text |
id | pubmed-2961751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29617512010-12-30 tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate Baharfar, Robabeh Vahdat, S. Mohammad Baghbanian, S. Meysam Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(18)O(6), a previously unknown coumarin derivative, the benzoyl substitutent makes a dihedral angle of 53.80 (16)° with the plane of the coumarin rings. An intramolecular O—H⋯O hydrogen bond is observed. International Union of Crystallography 2008-06-07 /pmc/articles/PMC2961751/ /pubmed/21202843 http://dx.doi.org/10.1107/S1600536808016188 Text en © Baharfar 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 Baharfar, Robabeh Vahdat, S. Mohammad Baghbanian, S. Meysam tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate |
title |
tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate |
title_full |
tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate |
title_fullStr |
tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate |
title_full_unstemmed |
tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate |
title_short |
tert-Butyl 6-benzoyl-5-hydroxy-2-oxo-2H-chromene-4-carboxylate |
title_sort | tert-butyl 6-benzoyl-5-hydroxy-2-oxo-2h-chromene-4-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961751/ https://www.ncbi.nlm.nih.gov/pubmed/21202843 http://dx.doi.org/10.1107/S1600536808016188 |
work_keys_str_mv | AT baharfarrobabeh tertbutyl6benzoyl5hydroxy2oxo2hchromene4carboxylate AT vahdatsmohammad tertbutyl6benzoyl5hydroxy2oxo2hchromene4carboxylate AT baghbaniansmeysam tertbutyl6benzoyl5hydroxy2oxo2hchromene4carboxylate |