Stereoselective and mild method for the synthesis of C-d-glucosylarenes in high yield
- 1 August 1989
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 191 (1) , 125-129
- https://doi.org/10.1016/0008-6215(89)85052-9
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- C-glycosidation of pyridyl thioglycosidesPublished by Elsevier ,2001
- Stereoselective synthesis of α- C-allyl-glycopyranosidesTetrahedron Letters, 1985
- Highly stereoselective c-allylation of glycopyranosides with allylsilanes catalyzed by silyl triflate or iodosilaneTetrahedron Letters, 1984
- Formation of convenient chiral intermediates from carbohydrates and their use in synthesisTetrahedron, 1984
- Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosidesJournal of the American Chemical Society, 1982
- C-glycosides from O-glycosyl trichloroacetimidatesTetrahedron Letters, 1982
- Synthesis of Naturally Occurring C-Nucleosides, Their Analogs, and Functionalized C-Glycosyl PrecursorsPublished by Elsevier ,1976
- Nouvelles methodes de -fonctionnalisation anomerique: acces aux precurseurs chimiques des -nucleosidesTetrahedron Letters, 1973
- 398. 2,3,4,6-Tetra-O-benzyl-D-glucosyl chloride and its use in the synthesis of the α- and β-anomers of 2-O-D-glucosylglycerol and 4-O-D-glucosyl-D-ribitolJournal of the Chemical Society, 1964