Cargando…
Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside
The pyranosyl ring in the title compound, C(16)H(18)O(5)S, adopts an envelope conformation, with the acetyl groups in equatorial positions. In the crystal, weak C—H⋯O interactions link the molecules into chains.
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247579/ https://www.ncbi.nlm.nih.gov/pubmed/22219884 http://dx.doi.org/10.1107/S1600536811040165 |
_version_ | 1782220139594252288 |
---|---|
author | Kinfe, Henok H. Mebrahtu, Fanuel M. Muller, Alfred |
author_facet | Kinfe, Henok H. Mebrahtu, Fanuel M. Muller, Alfred |
author_sort | Kinfe, Henok H. |
collection | PubMed |
description | The pyranosyl ring in the title compound, C(16)H(18)O(5)S, adopts an envelope conformation, with the acetyl groups in equatorial positions. In the crystal, weak C—H⋯O interactions link the molecules into chains. |
format | Online Article Text |
id | pubmed-3247579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32475792012-01-04 Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside Kinfe, Henok H. Mebrahtu, Fanuel M. Muller, Alfred Acta Crystallogr Sect E Struct Rep Online Organic Papers The pyranosyl ring in the title compound, C(16)H(18)O(5)S, adopts an envelope conformation, with the acetyl groups in equatorial positions. In the crystal, weak C—H⋯O interactions link the molecules into chains. International Union of Crystallography 2011-10-05 /pmc/articles/PMC3247579/ /pubmed/22219884 http://dx.doi.org/10.1107/S1600536811040165 Text en © Kinfe 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 Kinfe, Henok H. Mebrahtu, Fanuel M. Muller, Alfred Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
title | Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
title_full | Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
title_fullStr | Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
title_full_unstemmed | Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
title_short | Phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
title_sort | phenyl 4,6-di-o-acetyl-2,3-dideoxy-1-thio-α-d-erythro-hex-2-enopyranoside |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247579/ https://www.ncbi.nlm.nih.gov/pubmed/22219884 http://dx.doi.org/10.1107/S1600536811040165 |
work_keys_str_mv | AT kinfehenokh phenyl46dioacetyl23dideoxy1thioaderythrohex2enopyranoside AT mebrahtufanuelm phenyl46dioacetyl23dideoxy1thioaderythrohex2enopyranoside AT mulleralfred phenyl46dioacetyl23dideoxy1thioaderythrohex2enopyranoside |