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Regioselective glycosylation of fully unprotected methyl hexopyranosides by means of transient masking of hydroxy groups with arylboronic acids
Authors:Eisuke Kaji  Takashi Nishino  Koji Ishige  Yohei Ohya  Yuko Shirai
Institution:School of Pharmacy, Kitasato University, Shirokane 5-9-1, Minato-ku, Tokyo 108-8641, Japan
Abstract:Facile, one-pot synthesis was developed for several β(1→2)-, β(1→3)- or β(1→4)-linked disaccharides from fully unprotected methyl hexopyranosides according to the molecular recognition by arylboronic acids. The methodology was successfully applied to facile, short step assembly of the trisaccharide fragment of type II arabinogalactan.
Keywords:Oligosaccharide  Glycosylation  Regioselectivity  Masking  Arylboronate
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