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4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal
The title compound, C(20)H(36)O(6)S(4), was obtained by ethanethiolysis of 3,5,6-tri-O-acetyl-1,2-O-isopropylidene-α-d-glucofuranose. One of the ethyl groups is disordered over two sites with refined occupancies of 0.869 (6) and 0.131 (6). Compared with the precursor, the absolute configuration...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969703/ https://www.ncbi.nlm.nih.gov/pubmed/21583095 http://dx.doi.org/10.1107/S1600536809015694 |
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author | Xi, Xiao-Dong Shi, Da-Xin Li, Hui Li, Yun-Zheng Wu, Qin-Pei |
author_facet | Xi, Xiao-Dong Shi, Da-Xin Li, Hui Li, Yun-Zheng Wu, Qin-Pei |
author_sort | Xi, Xiao-Dong |
collection | PubMed |
description | The title compound, C(20)H(36)O(6)S(4), was obtained by ethanethiolysis of 3,5,6-tri-O-acetyl-1,2-O-isopropylidene-α-d-glucofuranose. One of the ethyl groups is disordered over two sites with refined occupancies of 0.869 (6) and 0.131 (6). Compared with the precursor, the absolute configuration of the stereocenters at positions C-3 and C-2 are inverted and maintained, respectively. |
format | Text |
id | pubmed-2969703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29697032010-12-30 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal Xi, Xiao-Dong Shi, Da-Xin Li, Hui Li, Yun-Zheng Wu, Qin-Pei Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(36)O(6)S(4), was obtained by ethanethiolysis of 3,5,6-tri-O-acetyl-1,2-O-isopropylidene-α-d-glucofuranose. One of the ethyl groups is disordered over two sites with refined occupancies of 0.869 (6) and 0.131 (6). Compared with the precursor, the absolute configuration of the stereocenters at positions C-3 and C-2 are inverted and maintained, respectively. International Union of Crystallography 2009-05-07 /pmc/articles/PMC2969703/ /pubmed/21583095 http://dx.doi.org/10.1107/S1600536809015694 Text en © Xi 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 Xi, Xiao-Dong Shi, Da-Xin Li, Hui Li, Yun-Zheng Wu, Qin-Pei 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
title | 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
title_full | 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
title_fullStr | 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
title_full_unstemmed | 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
title_short | 4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
title_sort | 4,5,6-tri-o-acetyl-2,3-di-s-ethyl-2,3-dithio-d-allose diethyl dithioacetal |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969703/ https://www.ncbi.nlm.nih.gov/pubmed/21583095 http://dx.doi.org/10.1107/S1600536809015694 |
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