A stereoselective synthesis of 2-acetamido-2-deoxy-C-glucosides: Glycosyl dianions as key intermediates
- 15 August 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (33) , 6067-6070
- https://doi.org/10.1016/0040-4039(94)88077-8
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthesis of C-glycosides of N-acetylglucosamine by direct alkylation of 2-amino-2-deoxy-2,3,4,6-tetra-O-acetyl glucopyranosyl chlorideTetrahedron Letters, 1994
- Direct coupling of functionalized organolithium compounds with aryl and vinyl halidesThe Journal of Organic Chemistry, 1993
- Biological roles of oligosaccharides: all of the theories are correctGlycobiology, 1993
- The synthesis of 2-azido C-glycosyl sugarsTetrahedron Letters, 1992
- Recent developments in the synthesis of C-glycosidesTetrahedron, 1992
- Synthesis of 2-amino C-glucosides and 2-amino C-glucosides spiroketalsTetrahedron Letters, 1991
- Preparation and some applications of functionalized organo-lithium compounds in organic synthesisPure and Applied Chemistry, 1990
- Fragmentation and wittig olefination of glucosamine derivatives-a simple route to open chain amino sugars and chiral glycerolsTetrahedron, 1988
- O‐Glycosylimidate, 19. Reaktionen von Glycosyl‐trichloracetimidaten mit silylierten C‐NucleophilenEuropean Journal of Organic Chemistry, 1985
- Syntheses with Partially Benzylated Sugars. VI.1 Some Solvolytic Reactions of 2-Acetamido-1-O-acyl-2-deoxy-D-glucopyranose and -D-galactopyranose DerivativesThe Journal of Organic Chemistry, 1966