A convenient synthesis of S-glycosyl donors of D-glucose and O-glycosylations involving the new reagent.
- 1 January 1990
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 38 (3), 636-638
- https://doi.org/10.1248/cpb.38.636
Abstract
The synthesis of S-glycosyl donors from 2, 3, 4, 6-tetra-O-benzyl-α-glucopyranose (1) using S, S'-bis(1-phenyl-1H-tetrazol-5-yl) dithiocarbonate (2) was carried out by a one-step reaction. One of the S-glycosyl donors, S-1-(1'-phenyl-1H-tetrazolyl)2, 3, 4, 6-tetra-O-benzyl-β-D-glucopyranose (3a), was utilized for glycosylation of glycosyl acceptors such as methanol or cholesterol using silver triflate as a promoter.Keywords
This publication has 4 references indexed in Scilit:
- A new method for the synthesis of O-glycosides from S-glycosidesThe Journal of Organic Chemistry, 1987
- Syntheses of 2-O-glycosyl derivatives of N-acetyl-d-neuraminic acidCarbohydrate Research, 1986
- Synthesis of a tetra- and a nona-saccharide which contain α-l-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteinsCarbohydrate Research, 1985
- A mild and general method for the synthesis of 0-glycosidesJournal of the American Chemical Society, 1983