696599-20-9

Upstream product

• 100-51-6 benzyl alcohol 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 100-39-0 benzyl bromide 
• 65877-63-6 3-O-benzyl-D-glucopyranose 
• 3282-30-2 pivaloyl chloride 
• 696599-12-9 benzyl 3-O-benzyl-α-D-glucopyranoside 
• 1216905-01-9 benzyl 3-O-benzyl-D-glucopyranoside 

Downstream Products

• 696599-36-7 benzyl-2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-[2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->4)]-3-O-benzyl-6-O-pivaloyl-α-D-glucopyranoside 
• 729599-35-3 benzyl 2,3,4-tri-O-acetyl-β-L-fucopyranosyl-(1->2)-[2,3,4,-tri-O-acetyl-β-L-fucopyranosyl-(1->4)]-3-O-benzyl-6-O-pivaloyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of chacotriose analogues

We report here the synthesis of three chacotriose analogues, namely β-L-fucopyranosyl-(1→2)-[β-L-fucopyranosyl-(1→4)] -D-glucopyranose, β-L-fucopyranosyl-(1→2)-[β-L-fucopyranosyl- (1→4)]-D-galactopyranose, and α-L-rhamnopyranosyl-(1→2)- [α-L-rhamnopyranos

An improved synthesis of chacotriose

Glycosylation using the trichloroacetimidate method was investigated in order to synthetize chacotriose. In a continuation of previous studies we present here a shorter approach to the synthesis of chacotriose, α-L-rhamnopyranosyl-(1→2)-[α:-L-rhamnopyranosyl-(1→4)] -D-glucopyranose.