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Enzymatic synthesis of p-nitrophenyl 45-O-β-d-galactosyl-α-maltopentaoside as a substrate for human α-amylases

✍ Scribed by Taichi Usui; Koichi Ogawa; Hiroyuki Nagai; Hidenori Matsui


Book ID
107719030
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
665 KB
Volume
202
Category
Article
ISSN
0003-2697

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p-Nitrophenyl alpha-maltopentaoside, having a benzyl group on O-6 of the terminal (nonreducing) D-glucosyl group was prepared by use of a reductive ring-opening reaction. Highly regioselective reduction of p-nitrophenyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-alpha-D-glucopyranosyl)-(1----4)- tris[O-(