187031-90-9

Upstream product

• 187031-80-7 phenyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-1-thio-β-D-galactopyranoside 
• 144830-21-7 phenyl 2,3-di-O-benzyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside 
• 231623-55-5 phenyl 2,3-di-O-benzyl-1-thio-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 187031-74-9 benzyl (benzyl 2,3-di-O-benzyl-β-D-galactopyranosid)uronate 
• 187031-83-0 (2S,3R,4S,5R,6S)-4,5-Bis-benzyloxy-3-(4-methoxy-benzyloxy)-6-phenylsulfanyl-tetrahydro-pyran-2-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

An efficient and highly stereoselective α(1 → 4) glycosylation between two D-galacturonic acid ester derivatives

The highly stereoselective α(1 → 4) coupling between two D-galacturonic acid ester derivatives was accomplished in good yields, for the first time, using a phenylthioglycoside as donor. The method was designed to prepare D-galacturonic acid oligomers with methyl ester groups in definite positions.