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rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol

The title racemic triquinane, C(14)H(14)Cl(2)O(2), is composed of four five-membered rings, one of which is a tetra­hydro­furan ring to which an allyl group on one side and a hydroxyl group on the other side are attached. The core of the triquinane unit has a cis–syn–cis configuration. In the crysta...

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Detalles Bibliográficos
Autores principales: Kotha, Sambasivarao, Ansari, Saima, Gupta, Naveen Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462309/
https://www.ncbi.nlm.nih.gov/pubmed/36337590
http://dx.doi.org/10.1107/S2414314621012608
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author Kotha, Sambasivarao
Ansari, Saima
Gupta, Naveen Kumar
author_facet Kotha, Sambasivarao
Ansari, Saima
Gupta, Naveen Kumar
author_sort Kotha, Sambasivarao
collection PubMed
description The title racemic triquinane, C(14)H(14)Cl(2)O(2), is composed of four five-membered rings, one of which is a tetra­hydro­furan ring to which an allyl group on one side and a hydroxyl group on the other side are attached. The core of the triquinane unit has a cis–syn–cis configuration. In the crystal, the mol­ecules are linked by pairwise O—H⋯O hydrogen bonds, generating inversion dimers featuring R (2) (2)(8) loops. [Image: see text]
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spelling pubmed-94623092022-11-04 rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol Kotha, Sambasivarao Ansari, Saima Gupta, Naveen Kumar IUCrdata Data Reports The title racemic triquinane, C(14)H(14)Cl(2)O(2), is composed of four five-membered rings, one of which is a tetra­hydro­furan ring to which an allyl group on one side and a hydroxyl group on the other side are attached. The core of the triquinane unit has a cis–syn–cis configuration. In the crystal, the mol­ecules are linked by pairwise O—H⋯O hydrogen bonds, generating inversion dimers featuring R (2) (2)(8) loops. [Image: see text] International Union of Crystallography 2021-12-16 /pmc/articles/PMC9462309/ /pubmed/36337590 http://dx.doi.org/10.1107/S2414314621012608 Text en © Kotha et al. 2021 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Kotha, Sambasivarao
Ansari, Saima
Gupta, Naveen Kumar
rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
title rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
title_full rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
title_fullStr rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
title_full_unstemmed rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
title_short rac-(2aS,2a(1) R,3aR,3a(1) S,5aS,6aR)-2a-Allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3aH-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
title_sort rac-(2as,2a(1) r,3ar,3a(1) s,5as,6ar)-2a-allyl-2,4-di­chloro-2a,2a(1),3a(1),5a,6,6a-hexa­hydro-3ah-3-oxadi­cyclo­penta­[cd,gh]penta­len-3a-ol
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462309/
https://www.ncbi.nlm.nih.gov/pubmed/36337590
http://dx.doi.org/10.1107/S2414314621012608
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