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3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne

The title compound, C(15)H(28)O(4), was prepared by the condensation of pivalaldehyde with penta­erythritol. In the crystal, the two halves of the mol­ecule are related by a crystallographic twofold rotation axis passing through the central spiro-C atom. The two non-planar six-membered heterocycles...

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Detalles Bibliográficos
Autores principales: Li, Zhengyi, Chen, Liang, Tang, Qiuzheng, Sun, Xiaoqiang
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011739/
https://www.ncbi.nlm.nih.gov/pubmed/21589636
http://dx.doi.org/10.1107/S1600536810049524
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author Li, Zhengyi
Chen, Liang
Tang, Qiuzheng
Sun, Xiaoqiang
author_facet Li, Zhengyi
Chen, Liang
Tang, Qiuzheng
Sun, Xiaoqiang
author_sort Li, Zhengyi
collection PubMed
description The title compound, C(15)H(28)O(4), was prepared by the condensation of pivalaldehyde with penta­erythritol. In the crystal, the two halves of the mol­ecule are related by a crystallographic twofold rotation axis passing through the central spiro-C atom. The two non-planar six-membered heterocycles both adopt chair conformations with the two tert-butyl groups both located in the equatorial positions.
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spelling pubmed-30117392010-12-30 3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne Li, Zhengyi Chen, Liang Tang, Qiuzheng Sun, Xiaoqiang Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(28)O(4), was prepared by the condensation of pivalaldehyde with penta­erythritol. In the crystal, the two halves of the mol­ecule are related by a crystallographic twofold rotation axis passing through the central spiro-C atom. The two non-planar six-membered heterocycles both adopt chair conformations with the two tert-butyl groups both located in the equatorial positions. International Union of Crystallography 2010-11-30 /pmc/articles/PMC3011739/ /pubmed/21589636 http://dx.doi.org/10.1107/S1600536810049524 Text en © Li et al. 2010 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
Li, Zhengyi
Chen, Liang
Tang, Qiuzheng
Sun, Xiaoqiang
3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
title 3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
title_full 3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
title_fullStr 3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
title_full_unstemmed 3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
title_short 3,9-Di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
title_sort 3,9-di-tert-butyl-2,4,8,10-tetra­oxaspiro­[5.5]undeca­ne
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011739/
https://www.ncbi.nlm.nih.gov/pubmed/21589636
http://dx.doi.org/10.1107/S1600536810049524
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