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ID 51556
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Author
Koga, Yuko
Kawamoto, Heizan
Yamamoto, Hiroshi
Abstract
Methyl 4-deoxy-4-dimethoxyphosphinoyl-2,3-O-isopropylidene-beta-D-ribopyranoside (12a) and methyl 2,4-dideoxy-4-dimethoxyphosphinoyl-beta-D-erythro-pentopyranoside (20) were efficiently prepared respectively from methyl 2,3-O-isopropylidene-beta-D-ribopyranoside (7a) and its 3,4-O-isopropylidene isomer (7b) in appreciably improved total yields compared with those via previously reported routes. Compounds (12a, 20) were led to D-ribofuranose and 2-deoxy-D-ribofuranose phospho sugars (4, 5).
Keywords
D-ribofuranose phospho sugar
2-deoxy-D-ribofuranose analog
C-P bond formation
stannylene acetal
Published Date
2007-12
Publication Title
Heterocycles
Volume
volume73
Issue
issue1
Start Page
581
End Page
591
ISSN
0385-5414
Content Type
Journal Article
Official Url
http://www.heterocycles.jp/newlibrary/libraries/abst/02617
language
English
Copyright Holders
© The Japan Institute of Heterocyclic Chemistry
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author
Refereed
True
DOI
Web of Science KeyUT