“…A similar protocol was applied to the regioselective removal of methyl ether protecting groups. 99 For per- O -methylated thioglucoside, primary methyl group was removed selectively and the respective 6- O -acetyl product was formed in 52% yield along with 3,6-di -O -acetyl compound was also formed as a minor side-product.…”
Section: Synthesis Of Partially Substituted Building Blocks By Regiosmentioning
Scope 1: sugar is uniformly protected leaving only one (or two) free hydroxyl group; scope 2: uniformly protected sugar is deprotected to liberate only one (or two) hydroxyl group.
“…A similar protocol was applied to the regioselective removal of methyl ether protecting groups. 99 For per- O -methylated thioglucoside, primary methyl group was removed selectively and the respective 6- O -acetyl product was formed in 52% yield along with 3,6-di -O -acetyl compound was also formed as a minor side-product.…”
Section: Synthesis Of Partially Substituted Building Blocks By Regiosmentioning
Scope 1: sugar is uniformly protected leaving only one (or two) free hydroxyl group; scope 2: uniformly protected sugar is deprotected to liberate only one (or two) hydroxyl group.
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