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• W2100287346 abstract "The O-allylphenyl (AP) anomeric moiety was investigated as a new leaving group that can be activated for chemical glycosylation under a variety of conditions, through both direct and remote pathways. Differentiation between the two activation pathways was achieved in a mechanistic study. The orthogonal-type activation of the AP moiety along with common thioglycosides allows for the execution of efficient oligosaccharide assembly." @default.
• W2100287346 created "2016-06-24" @default.
• W2100287346 creator A5021007518 @default.
• W2100287346 creator A5043089901 @default.
• W2100287346 date "2012-04-18" @default.
• W2100287346 modified "2023-10-01" @default.
• W2100287346 title "2-Allylphenyl glycosides as complementary building blocks for oligosaccharide and glycoconjugate synthesis" @default.
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• W2100287346 doi "https://doi.org/10.3762/bjoc.8.66" @default.
• W2100287346 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3343285" @default.
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