Cargando…
2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose
In the title compound, C(13)H(22)O(4), the acetonide ring adopts an envelope conformation with one of the O atoms as the flap atom, whereas a twisted conformation is found for the furanose ring. Centrosymmetric eight-membered {⋯OCOH}(2) synthons involving the hydroxy H and acetonide O atoms are fo...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972000/ https://www.ncbi.nlm.nih.gov/pubmed/21578847 http://dx.doi.org/10.1107/S1600536809048557 |
_version_ | 1782190720395771904 |
---|---|
author | Robinson, Tony V. Taylor, Dennis K. Tiekink, Edward R. T. |
author_facet | Robinson, Tony V. Taylor, Dennis K. Tiekink, Edward R. T. |
author_sort | Robinson, Tony V. |
collection | PubMed |
description | In the title compound, C(13)H(22)O(4), the acetonide ring adopts an envelope conformation with one of the O atoms as the flap atom, whereas a twisted conformation is found for the furanose ring. Centrosymmetric eight-membered {⋯OCOH}(2) synthons involving the hydroxy H and acetonide O atoms are found in the crystal structure. These are linked into a supramolecular chain in the a-axis direction via C—H⋯O contacts. |
format | Text |
id | pubmed-2972000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29720002010-12-30 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose Robinson, Tony V. Taylor, Dennis K. Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(22)O(4), the acetonide ring adopts an envelope conformation with one of the O atoms as the flap atom, whereas a twisted conformation is found for the furanose ring. Centrosymmetric eight-membered {⋯OCOH}(2) synthons involving the hydroxy H and acetonide O atoms are found in the crystal structure. These are linked into a supramolecular chain in the a-axis direction via C—H⋯O contacts. International Union of Crystallography 2009-11-21 /pmc/articles/PMC2972000/ /pubmed/21578847 http://dx.doi.org/10.1107/S1600536809048557 Text en © Robinson 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 Robinson, Tony V. Taylor, Dennis K. Tiekink, Edward R. T. 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose |
title | 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose |
title_full | 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose |
title_fullStr | 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose |
title_full_unstemmed | 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose |
title_short | 2-C-Cyclohexyl-2,3-O-isopropylideneerythrofuranose |
title_sort | 2-c-cyclohexyl-2,3-o-isopropylideneerythrofuranose |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972000/ https://www.ncbi.nlm.nih.gov/pubmed/21578847 http://dx.doi.org/10.1107/S1600536809048557 |
work_keys_str_mv | AT robinsontonyv 2ccyclohexyl23oisopropylideneerythrofuranose AT taylordennisk 2ccyclohexyl23oisopropylideneerythrofuranose AT tiekinkedwardrt 2ccyclohexyl23oisopropylideneerythrofuranose |