274692-87-4

Upstream product

• 274692-85-2 (1R,2R,3R,4R)-1,4-di-benzyloxy-2,3-(tert-butyldimethyl)silyloxy-5-methylenecyclohexane 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 188839-35-2 D-1,6-O-(1-methylethylidene)-2,5-bis-O-(phenylmethyl)-allo-inositol 
• 274692-78-3 (2R,3R,4R,5R)-2,5-di-benzyloxy-3,4-(isopropylidenedioxy)cyclohexan-1-one 
• 274692-79-4 (1R,2R,3R,4R)-1,4-di-benzyloxy-2,3-isopropylidenedioxy-5-methylenecyclohexane 
• 274692-80-7 (1R,2R,3R,4R)-1,4-di-benzyloxy-5-methylenecyclohexane-2,3-diol 
• 274692-75-0 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate 

Downstream Products

• 141436-56-8 1L-(1,2,3/4,5)-1-C-Methyl-2,3,4,5-cyclohexanetetrol 

Relevant academic research and scientific papers

Synthesis of carba- and C-fucopyranosides and their evaluation as α-fucosidase inhibitors - Analysis of an unusual conformation adopted by an amino-C-fucopyranoside

Several carba- and C-fucopyranosides bearing a variety of substituents at their pseudoanomeric positions have been synthesized and tested as inhibitors of bovine kidney a-fucosidase. From the IC50 values, some conclusions about the structure-ac

Stereoselective synthesis of carba- and C-glycosyl analogs of fucopyranosides

Fucopyranoside analogs with methylene groups instead of endo- or exo- anomeric oxygens, carba- and C-fucopyranosides, respectively, were synthesized. For the synthesis of 5a-carba-L-fucose (1) two approaches were studied, which shared a common cyclitol bu