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ID 44361
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Author
Baba, Hiroki
Yamamoto, Hiroshi
Abstract
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.
Keywords
Pterine Glycoside
Biopterin D-Glucoside
Pteridine
Selective α-Glycosylation
Protecting Group
Published Date
2009-02-01
Publication Title
Heterocycles
Volume
volume77
Issue
issue2
Publisher
The Japan Institute of Heterocyclic Chemistry
Start Page
747
End Page
753
ISSN
1881-0942
Content Type
Journal Article
Official Url
http://dx.doi.org/10.3987/COM-08-S(F)60
language
English
Copyright Holders
© The Japan Institute of Heterocyclic Chemistry
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author
Refereed
True
DOI
Web of Science KeyUT