Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside

In the chiral title compound, C(14)H(17)ClO(7)S, an inter­mediate in the synthesis of the AIDS treatment drug zidovudine, the threose ring adopts an envelope configuration, with the O atom at the flap position.

Detalles Bibliográficos
Autores principales: Jiang, Hongshi, Li, Hui, Sun, Hong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983765/
https://www.ncbi.nlm.nih.gov/pubmed/21580651
http://dx.doi.org/10.1107/S1600536810007087
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author Jiang, Hongshi
Li, Hui
Sun, Hong
author_facet Jiang, Hongshi
Li, Hui
Sun, Hong
author_sort Jiang, Hongshi
collection PubMed
description In the chiral title compound, C(14)H(17)ClO(7)S, an inter­mediate in the synthesis of the AIDS treatment drug zidovudine, the threose ring adopts an envelope configuration, with the O atom at the flap position.
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spelling pubmed-29837652010-12-30 Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside Jiang, Hongshi Li, Hui Sun, Hong Acta Crystallogr Sect E Struct Rep Online Organic Papers In the chiral title compound, C(14)H(17)ClO(7)S, an inter­mediate in the synthesis of the AIDS treatment drug zidovudine, the threose ring adopts an envelope configuration, with the O atom at the flap position. International Union of Crystallography 2010-03-13 /pmc/articles/PMC2983765/ /pubmed/21580651 http://dx.doi.org/10.1107/S1600536810007087 Text en © Jiang 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
Jiang, Hongshi
Li, Hui
Sun, Hong
Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside
title Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside
title_full Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside
title_fullStr Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside
title_full_unstemmed Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside
title_short Methyl 5-O-(4-chloro­benzo­yl)-2-de­oxy-3-O-methyl­sulfonyl-threo-pentofuran­oside
title_sort methyl 5-o-(4-chloro­benzo­yl)-2-de­oxy-3-o-methyl­sulfonyl-threo-pentofuran­oside
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983765/
https://www.ncbi.nlm.nih.gov/pubmed/21580651
http://dx.doi.org/10.1107/S1600536810007087
work_keys_str_mv AT jianghongshi methyl5o4chlorobenzoyl2deoxy3omethylsulfonylthreopentofuranoside
AT lihui methyl5o4chlorobenzoyl2deoxy3omethylsulfonylthreopentofuranoside
AT sunhong methyl5o4chlorobenzoyl2deoxy3omethylsulfonylthreopentofuranoside

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