Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate

The title compound, C(19)H(18)O(4), exhibits a long C—C bond [1.575 (2) Å] in the cage structure. In the crystal, pairs of O—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. C—H⋯O inter­actions also occur.

Detalles Bibliográficos
Autores principales: Karpoormath, Rajshekhar, Naicker, Tricia, Govender, Thavendran, Kruger, Hendrik G., Maguire, Glenn E. M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100052/
https://www.ncbi.nlm.nih.gov/pubmed/21754154
http://dx.doi.org/10.1107/S1600536811009020
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author Karpoormath, Rajshekhar
Naicker, Tricia
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
author_facet Karpoormath, Rajshekhar
Naicker, Tricia
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
author_sort Karpoormath, Rajshekhar
collection PubMed
description The title compound, C(19)H(18)O(4), exhibits a long C—C bond [1.575 (2) Å] in the cage structure. In the crystal, pairs of O—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. C—H⋯O inter­actions also occur.
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spelling pubmed-31000522011-07-13 Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate Karpoormath, Rajshekhar Naicker, Tricia Govender, Thavendran Kruger, Hendrik G. Maguire, Glenn E. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(18)O(4), exhibits a long C—C bond [1.575 (2) Å] in the cage structure. In the crystal, pairs of O—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. C—H⋯O inter­actions also occur. International Union of Crystallography 2011-03-12 /pmc/articles/PMC3100052/ /pubmed/21754154 http://dx.doi.org/10.1107/S1600536811009020 Text en © Karpoormath et al. 2011 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
Karpoormath, Rajshekhar
Naicker, Tricia
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
title Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
title_full Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
title_fullStr Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
title_full_unstemmed Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
title_short Benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
title_sort benzyl 5-hy­droxy-4-oxapenta­cyclo­[5.4.1.0(2,6).0(3,10).0(8,11)]dodecane-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100052/
https://www.ncbi.nlm.nih.gov/pubmed/21754154
http://dx.doi.org/10.1107/S1600536811009020
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AT govenderthavendran benzyl5hydroxy4oxapentacyclo54102603100811dodecane3carboxylate
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AT maguireglennem benzyl5hydroxy4oxapentacyclo54102603100811dodecane3carboxylate

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