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