ID | 51556 |
FullText URL | |
Author |
Koga, Yuko
Kawamoto, Heizan
Yamamoto, Hiroshi
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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).
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Keywords | D-ribofuranose phospho sugar
2-deoxy-D-ribofuranose analog
C-P bond formation
stannylene acetal
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Published Date | 2007-12
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Publication Title |
Heterocycles
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Volume | volume73
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Issue | issue1
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Start Page | 581
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End Page | 591
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ISSN | 0385-5414
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Content Type |
Journal Article
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Official Url | http://www.heterocycles.jp/newlibrary/libraries/abst/02617
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language |
English
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Copyright Holders | © The Japan Institute of Heterocyclic Chemistry
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File Version | author
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Refereed |
True
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DOI | |
Web of Science KeyUT |