270087-62-2

Upstream product

• 254444-15-0 Phenyl 3,4,6-tri-O-benzyl-1-seleno-2-O-allyloxycarbonyl-α-D-mannopyranoside 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 13242-53-0 acetobromomannose 
• 270087-67-7 ethyl 2-O-acetyl-3,4-di-O-benzyl-6-O-(tert-butyldimethylsilyl)-1-thio-α-D-mannopyranoside 
• 496812-18-1 ethyl 3,4-di-O-benzyl-6-O-(tert-butyldimethylsilyl)-1-thio-α-D-mannopyranoside 
• 270087-60-0 3,4-di-O-benzyl-6-O-(tert-butyldimethylsilyl)-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 29073-91-4 1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 
• 3254-16-8 3,4,6-tri-O-acetyl-1,2-O-(1-methoxyethylidene)-β-D-mannopyranose 

Downstream Products

• 270087-63-3 ethyl 3,4-di-O-benzyl-2-O-chloroacetyl-6-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-1-thio-α-D-mannopyranoside 

Relevant academic research and scientific papers

Rapid assembly of oligosaccharides: 1,2-Diacetal-mediated reactivity tuning in the coupling of glycosyl fluorides

This paper describes the application of 1,2-diacetal protecting groups to control the reactivity tuning of glycosyl fluorides in oligosaccharide coupling reactions. The synthetic potential of this new methodology is demonstrated by the 'one-pot' synthesis