212691-24-2

Upstream product

• 100-39-0 benzyl bromide 
• 99773-30-5 5,6-O-isopropylidene-D-galactose diethyl dithioacetal 
• 212691-20-8 1-O-benzoyl-2,3,4-tri-O-benzyl-5,6-O-isopropylidene-D-galactitol 
• 212691-14-0 2,3,4-tri-O-benzyl-5,6-O-isopropylidene-D-galactose diethyldithioacetal 
• 212691-17-3 2,3,4-tri-O-benzyl-5,6-O-isopropylidene-D-galactose 
• 14506-38-8 2,3,4-tri-O-benzyl-5,6-O-isopropylidene-D-galactitol 
• 212691-22-0 1-O-benzoyl-2,3,4-tri-O-benzyl-D-galactitol 

Downstream Products

• 212691-26-4 Benzoic acid (E)-(2S,3S,4S)-2,3,4-tris-benzyloxy-6-formylamino-6-(toluene-4-sulfonyl)-hex-5-enyl ester 
• 212691-28-6 (2S,3S,4S)-2,3,4-Tris-benzyloxy-4-(3H-imidazol-4-yl)-butan-1-ol 
• 212691-29-7 (6S,7R,8S)-6,7,8-Tris-benzyloxy-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine 

Relevant academic research and scientific papers

Synthesis of an imidazolo-L-lyxo-piperidinose derivative

Imidazolo-L-lyxo-piperidonose 4 was synthesised from the D-galactose derivative 8 by two reaction sequences, via removal of a terminal carbon atom, stepwise incorporation of an imidazole moiety, and eventually intramolecular S(N)2 reaction corresponding piperidine ring. Piperdine 4 proved to be a poor glycosidase inhibitor.