(3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one

In the title compound, C(10)H(15)NO(3), the central six-membered ring of the indolizine system adopts a chair conformation, while the oxopyrrolidine and hydro­furan rings attached to the indolizine ring system have envelope conformations. In the crystal, the mol­ecules form chains parallel to the b...

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Autores principales: Švorc, Ľubomír, Vrábel, Viktor, Žúžiová, Jozefína, Marchalín, Štefan, Kožíšek, Jozef
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977186/
https://www.ncbi.nlm.nih.gov/pubmed/21583447
http://dx.doi.org/10.1107/S1600536809024283
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author Švorc, Ľubomír
Vrábel, Viktor
Žúžiová, Jozefína
Marchalín, Štefan
Kožíšek, Jozef
author_facet Švorc, Ľubomír
Vrábel, Viktor
Žúžiová, Jozefína
Marchalín, Štefan
Kožíšek, Jozef
author_sort Švorc, Ľubomír
collection PubMed
description In the title compound, C(10)H(15)NO(3), the central six-membered ring of the indolizine system adopts a chair conformation, while the oxopyrrolidine and hydro­furan rings attached to the indolizine ring system have envelope conformations. In the crystal, the mol­ecules form chains parallel to the b axis via inter­molecular O—H⋯O hydrogen bonds. The absolute configuration was assigned from the synthesis.
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spelling pubmed-29771862010-12-30 (3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one Švorc, Ľubomír Vrábel, Viktor Žúžiová, Jozefína Marchalín, Štefan Kožíšek, Jozef Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(15)NO(3), the central six-membered ring of the indolizine system adopts a chair conformation, while the oxopyrrolidine and hydro­furan rings attached to the indolizine ring system have envelope conformations. In the crystal, the mol­ecules form chains parallel to the b axis via inter­molecular O—H⋯O hydrogen bonds. The absolute configuration was assigned from the synthesis. International Union of Crystallography 2009-07-01 /pmc/articles/PMC2977186/ /pubmed/21583447 http://dx.doi.org/10.1107/S1600536809024283 Text en © Švorc 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
Švorc, Ľubomír
Vrábel, Viktor
Žúžiová, Jozefína
Marchalín, Štefan
Kožíšek, Jozef
(3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one
title (3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one
title_full (3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one
title_fullStr (3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one
title_full_unstemmed (3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one
title_short (3aR,8aS,9S,9aR)-9-Hydroxy­perhydro­furo[3,2-f]indolizin-6-one
title_sort (3ar,8as,9s,9ar)-9-hydroxy­perhydro­furo[3,2-f]indolizin-6-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977186/
https://www.ncbi.nlm.nih.gov/pubmed/21583447
http://dx.doi.org/10.1107/S1600536809024283
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