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- W2041487917 abstract "An efficient glycosylation strategy was applied in the synthesis of β‐d‐glucopyranosyl‐(1→3)‐[α‐d‐arabinopyranosyl‐(1→4)]‐β‐d‐glucopyranosyl‐(1→3)‐β‐d‐glucopyranosyl‐(1→3)‐[α‐d‐arabinopyranosyl‐(1→6)]‐d‐glucopyranose to secure β‐d‐(1→3) glycosidic bond formation between glucopyranosyl residues. The new strategy using a 4,6‐O‐benzylidenated acceptor avoided generation of the α major isomer in the attempted β‐d‐(1→3) glycosylation under standard glycosylation conditions. The hexasaccharide we prepared showed about 30% tumor growth inhibition towards S180 model study." @default.
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- W2041487917 date "2003-01-08" @default.
- W2041487917 modified "2023-09-26" @default.
- W2041487917 title "Synthesis of Laminarin Oligosaccharide Derivatives Having<scp>d</scp>‐Arabinofuranosyl Side‐Chains" @default.
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- W2041487917 doi "https://doi.org/10.1081/car-120023470" @default.
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