274692-78-3

Upstream product

• 188839-35-2 D-1,6-O-(1-methylethylidene)-2,5-bis-O-(phenylmethyl)-allo-inositol 
• 274692-75-0 2,5-di-O-benzyl-1,6-O-isopropylidene-D-allo-inositol 3,4-cyclic sulfate 

Downstream Products

• 274692-79-4 (1R,2R,3R,4R)-1,4-di-benzyloxy-2,3-isopropylidenedioxy-5-methylenecyclohexane 
• 141436-56-8 1L-(1,2,3/4,5)-1-C-Methyl-2,3,4,5-cyclohexanetetrol 
• 141436-57-9 1L-(1,2,5/3,4)-5-C-Methyl-1,2,3,4-cyclohexanetetrol 
• 274692-80-7 (1R,2R,3R,4R)-1,4-di-benzyloxy-5-methylenecyclohexane-2,3-diol 
• 274692-87-4 2,3-(tert-butyldimethyl)silyloxy-5a-carba-α-L-fucopyranose 
• 274692-85-2 (1R,2R,3R,4R)-1,4-di-benzyloxy-2,3-(tert-butyldimethyl)silyloxy-5-methylenecyclohexane 

Relevant academic research and scientific papers

Synthesis of bioactive indolocarbazoles: Synthesis, nucleophilic ring-opening and chiral base desymmetrisation of a cyclic sulfate intermediate

A number of new functionalised bridged indolocarbazole systems have been prepared by ring-opening reactions of a key cyclic sulfate intermediate, prepared from the corresponding diol by the action of sulfuryl diimidazole and DBU. The same cyclic sulfate a

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