39824-24-3

Upstream product

• 54656-59-6 (2R,3S,4S,5R,6R)-2-(acetoxymethyl)-6-(cyclohexyloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 1190202-85-7 but-2-yn-1-yl β-D-galactopyranoside 
• 108-93-0 cyclohexanol 
• 151168-59-1 1-propynyl-β-D-galactopyranoside 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 

Relevant academic research and scientific papers

Glycosylation using unprotected alkynyl donors

(Chemical Equation Presented) Gold(III) activation of unprotected propargyl glycosyl donors has been shown to be effective for the synthesis of saccharides. Terminal propargyl glycosides of glucose, galactose, and mannose required heating at reflux in ace

Synthesis of deoxy derivatives of lactose and their hydrolysis by beta-galactosidase from E. coli.

Methyl 2-deoxy-alpha-lactoside, methyl 3-deoxy-beta-lactoside, 1,5-anhydro-4-O-beta-D-galactopyranosyl-D-glucitol and the 2-deoxy and 2,3-dideoxy derivatives of 1,5-anhydro-4-O-beta-D-galactopyranosyl-D-glucitol have been synthesized by deoxygenation of l