DEHYDRATIVE α-GLUCOSYLATION USING A MIXTURE OF p-NITROBENZENESULFONYL CHLORIDE, SILVER TRIFLUOROMETHANESULFONATE, N,N-DIMETHYLACETAMIDE, AND TRIETHYLAMINE
- 5 July 1982
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 11 (7) , 1039-1040
- https://doi.org/10.1246/cl.1982.1039
Abstract
Stereoselective synthesis of α-linked di- and trisaccharides is performed by the one-stage glucosylation using 2,3,4,6-tetra-O-benzyl-α-d-glucopyranose and a mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, N,N-dimethylacetamide, and triethylamine in dichloromethane.This publication has 6 references indexed in Scilit:
- The Glucosylation of Several Alcohols with Tetra-O-benzyl-α-d-glucopyranose and a Mixture of p-Nitrobenzenesulfonyl Chloride, Silver Trifluoromethanesulfonate, and TriethylamineBulletin of the Chemical Society of Japan, 1980
- Nouvelle méthode de synthèse Stéréosélective de glycosides. Syntèse des α,α-tréhalose, analogues galacto, manno et autres α-d-glycosidesCarbohydrate Research, 1980
- Glucosidation of Tetra-O-benzyl-α-d-glucose with Chlorosilane and Silver SulfonateBulletin of the Chemical Society of Japan, 1979
- Synthesis of glycosides: reactions of the anomeric hydroxyl group with nitrogen—phosphorus betainesCarbohydrate Research, 1977
- A new synthesis of glycosides. Reactions of trifluoromethanesulfonic anhydride at the anomeric centreCarbohydrate Research, 1976
- Synthesis of benzyl 2,3,6-tri-O-benzyl-α-dd-glucopyranoside and benzyl 6-O-allyl-2,4-di-O-benzyl-β-d-galactopyranosideCarbohydrate Research, 1976