2-C-Phenyl­erythrono-1,4-lactone

The title compound (systematic name: 3,4-dihydr­oxy-3-phenyl­furan-2-one), C(10)H(10)O(4), features a five-membered γ-lactone ring with an envelope conformation at the C atom carrying the hydr­oxy group without the phenyl substituent. In the crystal, supra­molecular chains mediated by O—H⋯O hydrogen...

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Detalles Bibliográficos
Autores principales: Robinson, Tony V., Taylor, Dennis K., Tiekink, Edward R. T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971982/
https://www.ncbi.nlm.nih.gov/pubmed/21578853
http://dx.doi.org/10.1107/S1600536809048478
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author Robinson, Tony V.
Taylor, Dennis K.
Tiekink, Edward R. T.
author_facet Robinson, Tony V.
Taylor, Dennis K.
Tiekink, Edward R. T.
author_sort Robinson, Tony V.
collection PubMed
description The title compound (systematic name: 3,4-dihydr­oxy-3-phenyl­furan-2-one), C(10)H(10)O(4), features a five-membered γ-lactone ring with an envelope conformation at the C atom carrying the hydr­oxy group without the phenyl substituent. In the crystal, supra­molecular chains mediated by O—H⋯O hydrogen bonding are formed along the a-axis direction. These are consolidated in the crystal structure by C—H⋯O contacts.
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spelling pubmed-29719822010-12-30 2-C-Phenyl­erythrono-1,4-lactone Robinson, Tony V. Taylor, Dennis K. Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound (systematic name: 3,4-dihydr­oxy-3-phenyl­furan-2-one), C(10)H(10)O(4), features a five-membered γ-lactone ring with an envelope conformation at the C atom carrying the hydr­oxy group without the phenyl substituent. In the crystal, supra­molecular chains mediated by O—H⋯O hydrogen bonding are formed along the a-axis direction. These are consolidated in the crystal structure by C—H⋯O contacts. International Union of Crystallography 2009-11-21 /pmc/articles/PMC2971982/ /pubmed/21578853 http://dx.doi.org/10.1107/S1600536809048478 Text en © Robinson 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
Robinson, Tony V.
Taylor, Dennis K.
Tiekink, Edward R. T.
2-C-Phenyl­erythrono-1,4-lactone
title 2-C-Phenyl­erythrono-1,4-lactone
title_full 2-C-Phenyl­erythrono-1,4-lactone
title_fullStr 2-C-Phenyl­erythrono-1,4-lactone
title_full_unstemmed 2-C-Phenyl­erythrono-1,4-lactone
title_short 2-C-Phenyl­erythrono-1,4-lactone
title_sort 2-c-phenyl­erythrono-1,4-lactone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971982/
https://www.ncbi.nlm.nih.gov/pubmed/21578853
http://dx.doi.org/10.1107/S1600536809048478
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AT taylordennisk 2cphenylerythrono14lactone
AT tiekinkedwardrt 2cphenylerythrono14lactone

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