532932-75-5

Upstream product

• 93367-10-3 (2S,3S)-3,4-epoxy-1,2-di-O-isopropylidenebutane-1,2-diol 
• 4039-83-2 3-(4-methoxybenzyloxy)propyne 

Downstream Products

• 532932-80-2 (4S)-4-[(1'S,3'Z,5'RS)-5'-hydroxy-5'-phenyl-1'-phenylsulfonyloxy-3'-pentenyl]-2,2-dimethyl-1,3-dioxolane 
• 532932-77-7 (4S)-4-[(1'S)-5'-hydroxy-1'-phenylsulfonyloxy-3'-pentynyl]-2,2-dimethyl-1,3-dioxolane 
• 532932-84-6 (2S,3S,4R,6R)-6-[(4'S)-2',2'-dimethyl-1',3'-dioxolan-4'-yl]-3-methoxy-2-phenyltetrahydro-2H-pyran-4-ol 
• 532932-78-8 (4S)-4-[(1'S,3'Z)-5'-hydroxy-1'-phenylsulfonyloxy-3'-pentenyl]-2,2-dimethyl-1,3-dioxolane 
• 532932-85-7 (2S,3R,4S,6R)-6-[(4'S)-2',2'-dimethyl-1',3'-dioxolan-4'-yl]-4-methoxy-2-phenyltetrahydro-2H-pyran-3-ol 
• 532932-79-9 (4S)-4-[(1'S,3'Z)-4'-formyl-1'-phenylsulfonyloxy-3'-butenyl]-2,2-dimethyl-1,3-dioxolane 
• 532932-76-6 (4S)-4-[(1'S)-5'-(4-methoxybenzyloxy)-1'-phenylsulfonyloxy-3'-pentynyl]-2,2-dimethyl-1,3-dioxolane 

Relevant academic research and scientific papers

Stereoselective synthesis of C-phenyl D- and L-glycero heptopyranosides

D- and L-glycero-C-Phenyl heptopyranosides 1, 2 and 3 are synthesized for the first time from (R)-glyceraldehyde and L-ascorbic acid derivatives. The main strategy involves intramolecular nucleophilic substitution and double bond functionalisation.