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- W2055181504 abstract "The tetrasaccharide α-d-Glcp-(1→4)-α-d-Xylp-(1→4)-α-d-Xylp-(1→4)-d-Glcp (1) has been synthesized, as a substrate analogue of alpha amylase, by silver perchlorate-catalyzed glycosylation of benzyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-α-d-xylopyranosyl)-β-d-glucopyranoside (30) with 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-d-glucopyranosyl)-α-d-xylopyranosyl chloride or by methyl triflate-promoted condensation of 30 with methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-d-glucopyranosyl)-1-thio-β-d-xylopyranoside, followed by removal of protecting groups of the resulting tetrasaccharide derivative 40." @default.
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- W2055181504 date "1990-07-01" @default.
- W2055181504 modified "2023-09-27" @default.
- W2055181504 title "Synthesis of O-α-d-glucopyranosyl-(1→4)-O-α-d-xylopyranosyl-(1→4)-O-α-d-xylopyranosyl-(1→4)-d-glucopyranose as a substrate analogue of alpha amylase" @default.
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- W2055181504 doi "https://doi.org/10.1016/0008-6215(90)84242-m" @default.
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