
| 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
|
| 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
|
| 巻 | 73巻
|
| 号 | 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 |