| 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
|
| Published Date | 2007-12
|
| Publication Title |
Heterocycles
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| Volume | volume73
|
| Issue | issue1
|
| 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
|
| language |
English
|
| Copyright Holders | © The Japan Institute of Heterocyclic Chemistry
|
| File Version | author
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| Refereed |
True
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| DOI | |
| Web of Science KeyUT |