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ID 44361
フルテキストURL
著者
Hanaya, Tadashi Department of Chemistry, Faculty of Science, Okayama University Kaken ID publons researchmap
Baba, Hiroki Department of Chemistry, Faculty of Science, Okayama University
Yamamoto, Hiroshi School of Pharmacy, Shujitsu University
抄録
A novel glycosyl donor, 4,6-di-O-acetyl-2,3-di-O-(4-methoxy-benzyl)-α-D-glucopyranosy bromide (15) was efficiently prepared from D-glucose in 8 steps. The first synthesis of 2’-O-(α-D-glucopyranosyl)biopterin (2) was achieved by treatment of the key precursor, N(2)-(N,N-dimethylamino- methylene)-1’-O-(4-methoxybenzyl)-3-[2-(4-nitrophenyl)ethyl]biopterin (6) with 15 in the presence of silver triflate and tetramethylurea, followed by removal of the protecting groups.
キーワード
Pterine Glycoside
Biopterin D-Glucoside
Pteridine
Selective α-Glycosylation
Protecting Group
発行日
2009-02-01
出版物タイトル
Heterocycles
77巻
2号
出版者
The Japan Institute of Heterocyclic Chemistry
開始ページ
747
終了ページ
753
ISSN
1881-0942
資料タイプ
学術雑誌論文
オフィシャル URL
http://dx.doi.org/10.3987/COM-08-S(F)60
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