222973-63-9

Upstream product

• 101242-41-5 methyl 2,3-di-O-benzoyl-4-O-trifluoromethylsulfonyl-α-L-arabinopyranoside 
• 222973-53-7 (1R,4R,5S,6R)-4,5,6-tribenzyloxycyclohex-2-ene-1-thiol 
• 38088-60-7 methyl 3,4-O-isopropylidene-β-L-arabinopyranoside 
• 222973-52-6 S-methyl S-<(1R,4R,5S,6R)-4,5,6-tribenzyloxycyclohex-2-en-1-yl> dithiocarbonate 
• 222973-58-2 methyl 2,3-di-O-benzoyl-β-L-arabinopyranozide 
• 98-88-4 benzoyl chloride 
• 222973-62-8 methyl 2-O-benzoyl-3,4-O-isopropylidene-α-L-arabinopyranoside 

Relevant academic research and scientific papers

Synthesis of carbasugar-containing non-glycosidically linked pseudodisaccharides and higher pseudooligosaccharides

This minireview covers synthetic methods towards carbasugar-containing non-glycosidically linked pseudodisaccharides or higher pseudooligosaccharides. Carbocyclic pyranose mimetics (saturated or unsaturated between C-5 and C-5a) are linked by ether, thioe

A synthesis of conduramine B and a 'condurithiol', useful molecules for studying the inhibition of β-xylosidases

Conduramine B and a 'condurithiol', namely (1S,2S,3R,6R)-6-aminocyclohex-4-ene-1,2,3-triol and 1R,2S,3R,6R)-6-sulfanylcyclohex-4-ene-1,2,3-triol, have been prepared by the thermal rearrangement of an acetimidate and a dithiocarbonate, respectively. Both the amine and the thiol are putative inhibitors of β-xylosidases and, in order to mimic the natural substrate more closely, an N- and an S-pseudo-disaccharide have been prepared.