86117-03-5

Upstream product

• 79936-13-3 benzyl exo-3,4-O-benzylidene-β-L-arabinopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 86049-06-1 benzyl endo-3,4-O-benzylidene-2-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-β-L-arabinopyranoside 
• 27539-69-1 benzyl 2-O-β-D-glucopyranosyl-β-L-arabinopyranoside 
• 86049-08-3 benzyl 4-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-β-L-arabinopyranoside 
• 86049-09-4 Acetic acid (2S,3R,4S,5S)-2,5-bis-benzyloxy-3-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

(13)C-NMR STUDY OF METHYL- AND BENZYL ETHERS OF L-ARABINOSE AND OLIGOSACCHARIDES HAVING L-ARABINOSE AT THE REDUCING END. SYNTHESIS OF 2-O-β-D-GLUCOPYRANOSYL-, 2-O-α-L-RHAMNOPYRANOSYL-, 3-O-β-D-GLUCOPYRANOSYL-2-O-α-L-RHAMNOPYRANOSYL- AND 4-O-β-D-GLUCOPYRAN

The reaction of benzyl exo-3,4-O-benzylidene-β-L-arabinopyranoside 1 with α-acetobromo-D-glucose 3 resulted in a mixture of two disaccharides, 5 and 6, in which the configuration of the acetal ring was different.The reaction of 1 with α-acetobromo-L-rhamn