113084-97-2

Upstream product

• 204068-81-5 2,6-anhydro-1-azido-3,4,5,7-tetra-O-benzyl-1-deoxy-D-glycero-D-guloheptitol 
• 500766-97-2 2,3,4,6-tetra-O-benzyl-α/β-D-glucopyranosyl cyanide 
• 204068-78-0 1-(O-p-toluenesulfonyl)-3,4,5,7-tetra-O-benzyl-2,6-anhydroglucoheptitol 
• 89064-71-1 β-C-(hydroxymethyl)-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 113019-43-5 2,3,4,6-tetra-O-benzyl-1-formyl-D-glucopyranose 

Downstream Products

• 204068-87-1 N-((2S,3S,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-ylmethyl)-formamide 
• 204068-91-7 (2R,3R,4R,5S,6S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-isocyanomethyl-tetrahydro-pyran 

Relevant academic research and scientific papers

Synthesis of thiourea-tethered C-glycosyl amino acids via isothiocyanate-amine coupling

A new class of C-glycosyl amino acids displaying a thiourea segment as a linker has been designed and synthesized by addition of peracetylated glycosylmethyl isothiocyanates to an amine-functionalized amino acid (N α-Fmoc-β-amino-l-alanine). Th

An access to glycoconjugate libraries through multicomponent reactions

Four-component reactions: The Ugi reaction of four suitably functionalized carbohydrate derivatives (as a per-O-benzylated amine, an aldehyde, a carboxylic acid, and an isocyanide) allow the effective assembly of diverse compound libraries. The complex gl