ID | 51556 |
フルテキストURL | |
著者 |
Koga, Yuko
Okayama Univ, Fac Sci, Dept Chem
Kawamoto, Heizan
Okayama Univ, Fac Sci, Dept Chem
Yamamoto, Hiroshi
Okayama Univ, Fac Sci, Dept Chem
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抄録 | 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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キーワード | D-ribofuranose phospho sugar
2-deoxy-D-ribofuranose analog
C-P bond formation
stannylene acetal
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発行日 | 2007-12
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出版物タイトル |
Heterocycles
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巻 | 73巻
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号 | 1号
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開始ページ | 581
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終了ページ | 591
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ISSN | 0385-5414
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資料タイプ |
学術雑誌論文
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オフィシャル URL | http://www.heterocycles.jp/newlibrary/libraries/abst/02617
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言語 |
英語
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著作権者 | © The Japan Institute of Heterocyclic Chemistry
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論文のバージョン | author
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査読 |
有り
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DOI | |
Web of Science KeyUT |