SEARCH Articles Figures Tables 0-Glycosyl trichloroacetimidates, reactions 1.3- Oxazolines via iodocyclization of trichloroacetimidates 4-Methoxybenzyl-2,2,2-trichloroacetimidate A-Trichloroacetimidates Activations trichloroacetimidates Alkyl trichloroacetimidates Allyl 22.2-trichloroacetimidate Allylic trichloroacetimidate Allylic trichloroacetimidates Allylic trichloroacetimidates 3.3] sigmatropic rearrangement Benzyl 2,2,2-Trichloroacetimidate hydroxy group protection Benzyl trichloroacetimidate Esterification with 2,2,2-trichloroacetimidate Ethers Benzyl trichloroacetimidate From mannosyl trichloroacetimidates Galactose trichloroacetimidate Galactosyl trichloroacetimidate donor Geraniol trichloroacetimidate Glucosyl trichloroacetimidates, reaction Glucuronic acid, trichloroacetimidates Glycosidation trichloroacetimidates Glycosides trichloroacetimidates Glycosyl donors trichloroacetimidate Glycosyl trichloroacetimidate Glycosyl trichloroacetimidates Glycosyl trichloroacetimidates automated solid-phase synthesis Glycosyl trichloroacetimidates promoters Glycosyl trichloroacetimidates trisaccharide synthesis using Glycosylation trichloroacetimidates Glycosylation with glycosyl trichloroacetimidates Inverse procedure, trichloroacetimidates Mannopyranosyl trichloroacetimidate Mannose trichloroacetimidate Natural products trichloroacetimidates Neighboring-group participation trichloroacetimidate O-Galactosyl trichloroacetimidates O-Glucosyl trichloroacetimidates O-Glycosyl trichloroacetimidates Oligosaccharide synthesis with trichloroacetimidates Oligosaccharide synthesis with trichloroacetimidates activation Oligosaccharide synthesis with trichloroacetimidates disaccharides Oligosaccharide synthesis with trichloroacetimidates formation Oligosaccharide synthesis with trichloroacetimidates hexasaccharide P-Trichloroacetimidates Pentasaccharide trichloroacetimidate Polyprenyl phosphates from prenyl trichloroacetimidates Preparation of trichloroacetimidates Protection Benzyl trichloroacetimidate Rearrangement trichloroacetimidate Rhamnosyl trichloroacetimidate Saccharides trichloroacetimidates Saccharides via trichloroacetimidates Schmidt s trichloroacetimidate glycosidation Schmidt trichloroacetimidate Schmidt trichloroacetimidate method Schmidt trichloroacetimidate methodolog Schmidts trichloroacetimidate glycosidation Schmidts trichloroacetimidate glycosidation reaction Schmidt’s trichloroacetimidate Schmidt’s trichloroacetimidate glycosidation reaction Stereoselectivity glycosylations, trichloroacetimidates Sulfoxide and trichloroacetimidate The Trichloroacetimidate Method Thionocarbonates trichloroacetimidate Trichloroacetimidate Trichloroacetimidate Trichloroacetimidate approach Trichloroacetimidate approach synthesis Trichloroacetimidate chemistry Trichloroacetimidate donor, Trichloroacetimidate donors trichloroacetimidates Trichloroacetimidate formation Trichloroacetimidate intermediate Trichloroacetimidate method Trichloroacetimidate method condensation Trichloroacetimidate method in oligoheptose synthesis Trichloroacetimidate procedure Trichloroacetimidates formation Trichloroacetimidates from allylic alcohols Trichloroacetimidates glycosyl donor Trichloroacetimidates method Trichloroacetimidates reaction Trichloroacetimidates rearrangement Trichloroacetimidates, glycosylations, silver Trichloroacetimidates, glycosylations, silver trifluoromethanesulfonate Trichloroacetimidates, synthesis Trichloroacetimidic esters Trichloroacetimidic esters, Overman Trichloroacetimidic esters, Overman rearrangement