170452-34-3Relevant academic research and scientific papers
Synthesis of a thio analogue of n-propyl kojibioside, a potential glucosidase inhibitor
Andrews, John S.,Pinto, B. Mario
, p. 51 - 62 (2007/10/02)
The disaccharide α-D-Glc p-(1-S-2)-β-D-Glc p-(1-OPr) 1, a thio analogue of α-D-Glc p-(12)-α-D-Glc p-(1-OPr)(n-propyl kojibioside) in which the inter-glycosidic oxygen atom is replaced by sulfur, has been synthesized for evaluation as a potential glucosidase inhibitor.Glycosylation of the 2-thiol glucopyranosyl acceptor 4 with the trichloroacetimidate of 2,3,4,6-tetra-O-benzyl-α-D-glucopyranose 5 gave the α-linked disaccharide 6 stereoselectively.Deprotection was performed by hydrogenolysis in the presence of Pd/C to give 1 as the β-n-propyl glycoside.Glycosyl ation of the thiol 4 with the trichloroacetimidate of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranose 8 gave a 1:2.3 mixture of the α and β disaccharides (9 and 10); evidence is presented for the occurrence of the orthoester 11, as an intermediate in the formation of the β-disaccharide. Keywords: Thio analogue; n-Propyl kojibioside; Glucosidase inhibitor
