93237-54-8

Upstream product

• 132074-89-6 methyl 4,6-O-benzylidene-2,3-dideoxy-α-D-threo-hex-2-enoside 
• 132074-90-9 methyl 4,6-O-benzylidene-2,3-di-O-[(methylthio)thiocarbonyl]-α-D-galactopyranoside 
• 64552-06-3 methyl 4,6-O-benzylidene-α-D-galactopyranoside 
• 1373344-40-1 C₂₁H₂₂O₆S 
• 221662-13-1 methyl 2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside 
• 21193-75-9 D-galactal 
• 18968-72-4 methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-threo-hex-2-enopyranoside 
• 93237-53-7 methyl 4,6-O-benzylidene-2,3-di-O-(N-imidazoylsulfonyl)-β-D-galactopyranoside 
• 3162-96-7 methyl 4,6-O-benzylidene-β-D-galactopyranoside 

Downstream Products

• 131985-37-0 (4R,5R)-4,6-dibenzyloxy-5-hydroxyhexanal ethylene dithioacetal 
• 131985-40-5 (4R,5S)-5-azido-4,6-dibenzyloxyhexanal 
• 131985-38-1 2-mercaptoethyl 4,6-di-O-benzyl-1-thio-1,2,3-trideoxy-α-D-threo-hexoside 
• 131985-39-2 (4R,5S)-5-azido-4,6-dibenzyloxyhexanal ethylene dithioacetal 
• 132023-36-0 (4R,5R)-4,6-dibenzyloxy-5-p-toluenesulfonyloxyhexanal ethylene dithioacetal 
• 131985-35-8 methyl 4,6-di-O-benzyl-2,3-dideoxy-α-D-threo-hexopyranoside 
• 93302-30-8 methyl 4-O-benzoyl-2,3,6-trideoxy-β-D-threo-hexopyranoside 
• 93302-29-5 methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-β-D-threo-hexopyranoside 

Relevant academic research and scientific papers

Bromodimethylsulfonium bromide catalyzed synthesis of methyl 2-dexoy-4,6-o-benzylidene galactopyranoside from galactal and the rapid route to 2,3- and 2,6-dideoxygalactopyranoses

4,6-O-Benzylidenation of D-galactal with PhCH(OCH3)2 catalyzed by bromodimethylsulfonium bromide leads to methyl 2-dexoy-4,6-O- benzylidene galactopyranoside efficiently, which serves as a key intermediate to the ready preparation of

The Synthesis of (2S,3R)-2-Hydroxymethylpiperidin-3-ol, a Fragment of the Alakloid Swainsonine

Methyl α- and β-D-galactopyranoside have been converted into methyl 4,6-di-O-benzyl-2,3-dideoxy-α- and -β-D-threo-hexoside, and subsequent treatment with ethanedithiol gives the same alcohol.Tosylation and azide displacement gives, after hydrolysis, an az

Synthesis of Tetrasaccharides Related to the O-Specific Determinants of Salmonella Serogroups A, B and D1

The branched tetrasaccharides, 4-O-(3-O-(deoxy-α-D-hexopyranosyl)-2-O-(α-D-galactopyranosyl)-α-D-mannopyranosyl)-α-L-rhamnopyranose, with the deoxy-α-D-hexopyranosyl equal to 3,6-dideoxy-α-D-ribo-hexopyranose, 3,6-dideoxy-α-D-arabino-hexopyranose, 3,6-did