2,3-Unsaturated allyl glycosides as glycosyl donors for selective α-glycosylation
Brijesh Kumar1, Mushtaq A Aga, Abdul Rouf
1Bio-organic Chemistry Division, Indian Institute of Integrative Medicine (CSIR), Canal Road, Jammu, India-180001.
Abstract:
In the presence of NBS and a catalytic amount of a Lewis acid, 2,3-unsaturated allyl glycosides [6-(allyloxy)-3,6-dihydro-2-(hydroxymethyl)-2H-pyran-3-ol] have been successfully used as versatile glycosyl donors for the stereoselective α-glycosylation of a variety of alcohols comprising sensitive functions such as acetonide, keto, nitro, and ester in 50-90% yields. The methodology offers an equally facile alternative to 4-pentenyl replacement in unsaturated sugars.
Related Concept Videos
Oligosaccharide Assembly
Multiple sugar molecules that may or may...
Protein Glycosylation
Glycosylation occurs in...
Conjugate Addition to α,β-Unsaturated Carbonyl Compounds
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Proteoglycans
Aldehydes and Ketones with Alcohols: Hemiacetal Formation


