679430-83-2

Upstream product

• 64-19-7 acetic acid 
• 679430-81-0 1-azido-2,3,4-tri-O-benzyl-α-L-fucopyranose 
• 250691-61-3 (2S,3S,4R,5R,6S)-3,4,5-Tris-benzyloxy-2-iodo-6-methyl-tetrahydro-pyran 
• 289884-68-0 acetyl o-diphenylphosphinophenyl ether 
• 289884-69-1 2-diphenylphosphino-N-acetylimidazole 
• 507-09-5 tiolacetic acid 
• 83562-59-8 1-O-acetyl-2,3,4-tri-O-benzyl-α-L-fucopyranose 

Relevant academic research and scientific papers

Selective synthesis of anomeric α-glycosyl acetamides via intramolecular Staudinger ligation of the α-azides

α-Glycosyl azides can be transformed into the corresponding α-glycosyl acetamides with complete retention of configuration via reduction-acylation (Staudinger ligation) reactions using specifically functionalized phosphines. The α-acetamides of per-O-benz