855269-58-8

Upstream product

• 67814-68-0 2,3-O-isopropylidene-D-ribofuranose 
• 532-20-7 D-Ribose 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 217309-46-1 5-(tert-butyldimethylsilyloxy)-2,3-isopropylidenedioxy-D-ribofuranose 
• 100-39-0 benzyl bromide 
• 116669-77-3 (1R,4'R,5'S)-(-)-1-(2',2'-dimethyl-5'-vinyl-1',3'-dioxolan-4'-yl)-2-(tert-butyldimethylsilyloxy)-1(R)-ethan-1-ol 

Downstream Products

• 201157-33-7 (2R,4'R,5'S)-(-)-2-(benzyloxy)-2-[2',2'-dimethyl-5'-vinyl-1',3'-dioxolan-4'-yl]-ethan-1-ol 

Relevant academic research and scientific papers

Palladium(II)-catalyzed intramolecular aminoacetoxylation of sugar derived alkenyl tosylsulfonamide: Total synthesis of L-deoxyallonojirimycin

Palladium catalyzed intramolecular aminoacetoxylation of D-ribose derived alkenyl tosylsulfonamide to deliver L-deoxyallonojirimycin in an overall yield of 19%. The preliminary screening of L-deoxyallonojirimycin against carbohydrate processing enzymes showed moderate inhibitory activity against α-glucosidase (yeast) and α-mannosidases.

A chiron approach to (1R,2R,5S,7S)-2-hydroxy-exo-brevicomin: A component of the volatiles produced by the male mountain pine beetle, Dendroctonus ponderosae

A chiron approach for the synthesis of (1R,2R,5S,7S)-2-hydroxy-exo- brevicomin 1, a component of the volatiles obtained from male mountain pine beetles, Dendroctonus ponderosae has been achieved. Our synthesis started with commercially available d-ribose