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(4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid

The asymmetric unit of the title compound, C(17)H(15)NO(4), contains two independent mol­ecules with similar geometric parameters. In both mol­ecules, the conformation of the cyclo­hexene ring is half-chair, while the pyrrolidinone ring adopts an envelope conformation with the γ-carbon atom of the α...

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Autores principales: Horak, Yuriy I., Lytvyn, Roman Z., Zubkov, Fedor I., Nikitina, Eugeniya V., Homza, Yuriy V., Lis, Tadeusz, Kinzhybalo, Vasyl, Obushak, Mykola D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569801/
https://www.ncbi.nlm.nih.gov/pubmed/23424547
http://dx.doi.org/10.1107/S160053681300144X
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author Horak, Yuriy I.
Lytvyn, Roman Z.
Zubkov, Fedor I.
Nikitina, Eugeniya V.
Homza, Yuriy V.
Lis, Tadeusz
Kinzhybalo, Vasyl
Obushak, Mykola D.
author_facet Horak, Yuriy I.
Lytvyn, Roman Z.
Zubkov, Fedor I.
Nikitina, Eugeniya V.
Homza, Yuriy V.
Lis, Tadeusz
Kinzhybalo, Vasyl
Obushak, Mykola D.
author_sort Horak, Yuriy I.
collection PubMed
description The asymmetric unit of the title compound, C(17)H(15)NO(4), contains two independent mol­ecules with similar geometric parameters. In both mol­ecules, the conformation of the cyclo­hexene ring is half-chair, while the pyrrolidinone ring adopts an envelope conformation with the γ-carbon atom of the α-pyrrolidinone ring as the flap. In the crystal, O—H⋯O hydrogen bonds between the carb­oxylic and carbonyl groups link alternate independent mol­ecules into chains propagating in the b-axis direction. The crystal packing also features weak C—H⋯π inter­actions.
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spelling pubmed-35698012013-02-19 (4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid Horak, Yuriy I. Lytvyn, Roman Z. Zubkov, Fedor I. Nikitina, Eugeniya V. Homza, Yuriy V. Lis, Tadeusz Kinzhybalo, Vasyl Obushak, Mykola D. Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(17)H(15)NO(4), contains two independent mol­ecules with similar geometric parameters. In both mol­ecules, the conformation of the cyclo­hexene ring is half-chair, while the pyrrolidinone ring adopts an envelope conformation with the γ-carbon atom of the α-pyrrolidinone ring as the flap. In the crystal, O—H⋯O hydrogen bonds between the carb­oxylic and carbonyl groups link alternate independent mol­ecules into chains propagating in the b-axis direction. The crystal packing also features weak C—H⋯π inter­actions. International Union of Crystallography 2013-01-23 /pmc/articles/PMC3569801/ /pubmed/23424547 http://dx.doi.org/10.1107/S160053681300144X Text en © Horak et al. 2013 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
Horak, Yuriy I.
Lytvyn, Roman Z.
Zubkov, Fedor I.
Nikitina, Eugeniya V.
Homza, Yuriy V.
Lis, Tadeusz
Kinzhybalo, Vasyl
Obushak, Mykola D.
(4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid
title (4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid
title_full (4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid
title_fullStr (4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid
title_full_unstemmed (4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid
title_short (4R*,4aR*,7aS*)-5-Oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4H-furo[2,3-f]isoindole-4-carb­oxy­lic acid
title_sort (4r*,4ar*,7as*)-5-oxo-6-phenyl-4a,5,6,7,7a,8-hexa­hydro-4h-furo[2,3-f]isoindole-4-carb­oxy­lic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569801/
https://www.ncbi.nlm.nih.gov/pubmed/23424547
http://dx.doi.org/10.1107/S160053681300144X
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