Tris(pentafluorophenyl)borane-promoted stereoselective glycosylation with glycosyl trichloroacetimidates under mild conditions

dc.contributor.author	Mishra K.B.; Singh A.K.; Kandasamy J.
dc.date.accessioned	2025-05-24T09:32:05Z
dc.description.abstract	Tris(pentafluorophenyl)borane-promoted stereoselective glycosylation with trichloroacetimidate glycosyl donors is described. The reactions proceed efficiently with a wide range of acceptors, from sugar to nonsugar, under mild conditions in the presence of a catalytic amount of B(C6F5)3. The perbenzylated glucosyl α-imidate provides β-selective glycosides in 70-92% yields. © 2018 American Chemical Society.
dc.identifier.doi	https://doi.org/10.1021/acs.joc.8b00215
dc.identifier.uri	http://172.23.0.11:4000/handle/123456789/17743
dc.relation.ispartofseries	Journal of Organic Chemistry
dc.title	Tris(pentafluorophenyl)borane-promoted stereoselective glycosylation with glycosyl trichloroacetimidates under mild conditions

Collections