anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol

The title compound, C(10)H(12)O(2), was synthesized as a candidate for further functionalization. The asymmetric unit comprises two independent mol­ecules, both of which are situated on a center of symmetry. Both mol­ecules are involved in a network of hydrogen bonding, with each alcohol group parti...

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Detalles Bibliográficos
Autores principales: Harris, Andria D., Baucom, Amy D., Sierra, Maria del Rosario I. Amado, Jones, Daniel S., Etzkorn, Markus
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959889/
https://www.ncbi.nlm.nih.gov/pubmed/21581251
http://dx.doi.org/10.1107/S1600536808035423
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author Harris, Andria D.
Baucom, Amy D.
Sierra, Maria del Rosario I. Amado
Jones, Daniel S.
Etzkorn, Markus
author_facet Harris, Andria D.
Baucom, Amy D.
Sierra, Maria del Rosario I. Amado
Jones, Daniel S.
Etzkorn, Markus
author_sort Harris, Andria D.
collection PubMed
description The title compound, C(10)H(12)O(2), was synthesized as a candidate for further functionalization. The asymmetric unit comprises two independent mol­ecules, both of which are situated on a center of symmetry. Both mol­ecules are involved in a network of hydrogen bonding, with each alcohol group participating in one hydrogen bond as a donor and in a second hydrogen bond as an acceptor.
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spelling pubmed-29598892010-12-30 anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol Harris, Andria D. Baucom, Amy D. Sierra, Maria del Rosario I. Amado Jones, Daniel S. Etzkorn, Markus Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(12)O(2), was synthesized as a candidate for further functionalization. The asymmetric unit comprises two independent mol­ecules, both of which are situated on a center of symmetry. Both mol­ecules are involved in a network of hydrogen bonding, with each alcohol group participating in one hydrogen bond as a donor and in a second hydrogen bond as an acceptor. International Union of Crystallography 2008-11-08 /pmc/articles/PMC2959889/ /pubmed/21581251 http://dx.doi.org/10.1107/S1600536808035423 Text en © Harris et al. 2008 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
Harris, Andria D.
Baucom, Amy D.
Sierra, Maria del Rosario I. Amado
Jones, Daniel S.
Etzkorn, Markus
anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
title anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
title_full anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
title_fullStr anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
title_full_unstemmed anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
title_short anti-Tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
title_sort anti-tricyclo­[4.2.1.1(2,5)]deca-3,7-diene-9-endo,10-endo-diol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959889/
https://www.ncbi.nlm.nih.gov/pubmed/21581251
http://dx.doi.org/10.1107/S1600536808035423
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