862973-11-3

Upstream product

• 82042-36-2 (E)-1,3,4-trideoxy-5,6-O-isopropylidene-3-C-methyl-D-glycero-hex-3-eno-2-ulose 
• 862973-12-4 (4R,5R)-4-acetyl-5-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-4-methyl-2-cyclohexen-1-one 
• 862973-15-7 1-[(1R,2R)-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-4,4-dimethoxy-1-methylcyclohexyl]ethan-1-one 
• 862973-14-6 (3R,4R)-4-acetyl-3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-4-methylcyclohexan-1-one 

Downstream Products

• 862973-16-8 (4S)-4-[(1R,2R)-2-[(1E)-2-iodo-1-propenyl]-5,5-dimethoxy-2-methylcyclohexyl]-2,2-dimethyl-1,3-dioxolane 

Relevant academic research and scientific papers

Synthetic studies toward GKK1032s, novel antibiotic antitumor agents: Enantioselective synthesis of the fully elaborated tricyclic core via an intramolecular Diels-Alder cycloaddition

An enantioselective synthesis of the fully elaborated tricyclic decahydrofluorene core (ABC-ring system) of GKK1032s, novel antimicrobial and antitumor agents, has been accomplished for the first time by employing a highly diastereoselective intramolecula

Enantioselective synthesis of the tricyclic core of GKK1032, novel antibiotic anti-tumor agents, by employing an intramolecular Diels-Alder cycloaddition strategy

An efficient and enantioselective synthesis of a decahydrofluorene nucleus, the tricyclic core (ABC-ring system) of GKK1032s, novel antimicrobial and anti-tumor agents, was achieved using a highly diastereoselective intramolecular Diels-Alder (IMDA) react