Alkyl sulfenyl triflate as activator in the thioglycoside-mediated formation of β-glycosidic linkages during oligosaccharide synthesis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference21 articles.
1. Thioglycosides as glycosylating agents in oligosaccharide synthesis
2. Syntheses of a branched heptasaccharide having phytoalexin-elicitor activity
3. A novel promoter for the efficient construction of 1,2-trans linkages in glycoside synthesis, using thioglycosides as glycosyl donors
4. Synthesis of 1,2--linked glycosides using dimethyl(methylthio) sulfonium triplate as promoter and thioglycosides as glycosyl donors
5. An efficient approach to O-glycosides through CuBr2-Bu4NBr mediated activation of glycosides
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1. Thioglycoside-based glycosylations in oligosaccharide synthesis;Synthetic Strategies in Carbohydrate Chemistry;2024
2. Cooperatively Catalyzed Activation of Thioglycosides That Bypasses Intermediacy of Glycosyl Halides;Chemistry – A European Journal;2023-07-03
3. Transition‐Metal‐Mediated Glycosylation with Thioglycosides;Chemistry – A European Journal;2022-01-12
4. Sequential activation of thioglycosides enables one-pot glycosylation;Organic Chemistry Frontiers;2021
5. Bismuth(iii) triflate as a novel and efficient activator for glycosyl halides;Organic & Biomolecular Chemistry;2021
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