“…Under both conditions azide 3 was completely stable (Scheme 2). Subsequently, the regioselectivity for benzyl groups 21 was probed with the dibenzylated azide 4. 22 In the case of DMDO two products were obtained.…”
When using benzyl ethers as permanent protecting groups in oligosaccharide synthesis selective oxidative debenzylation with NaBrO(3) + Na(2)S(2)O(4) under biphasic conditions is efficient and compatible with anomeric azides and many other functions.
“…Under both conditions azide 3 was completely stable (Scheme 2). Subsequently, the regioselectivity for benzyl groups 21 was probed with the dibenzylated azide 4. 22 In the case of DMDO two products were obtained.…”
When using benzyl ethers as permanent protecting groups in oligosaccharide synthesis selective oxidative debenzylation with NaBrO(3) + Na(2)S(2)O(4) under biphasic conditions is efficient and compatible with anomeric azides and many other functions.
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