200409-81-0

Upstream product

• 1303528-36-0 (5S,6S)-5-allyloxy-2-dihydroxyboryl-6-methyl-2-cyclohexen-1-one 
• 1303528-28-0 (4E,7S)-N-[(Z)-3-chloro-2-iodoprop-2-ene]-7-methoxy-N-methyltetradec-4-enamide 
• 1303528-30-4 (5S,6S)-5-methoxymethoxy-6-methylcyclohex-2-enone 
• 1303528-31-5 (5S,6S)-2-bromo-5-methoxymethoxy-6-methylcyclohex-2-enone 
• 1303528-33-7 (9S,10S)-6-bromo-10-methyl-9-trimethylsilyloxy-spiro[4.5]dec-6-ene 
• 1303528-34-8 (9S,10S)-6-bromo-9-hydroxy-10-methylspiro[4.5]dec-6-ene 
• 1303528-35-9 (9S,10S)-9-allyloxy-6-bromo-10-methylspiro[4.5]dec-6-ene 
• 1303528-37-1 (4E,7S)-N-{(2Z)-[(3S,4S)-4-allyloxy-3-methyl-2-oxocyclohex-1-enyl]-2-chloromethyleneethyl}-N-methyl-7-methoxytetradec-4-enamide 
• 2244-16-8 (S)-p-mentha-6,8-dien-2-one 
• 127853-80-9 (2S,3S,5S)-3-Hydroxy-2-methyl-5-(1-methylethenyl)cyclohexanone 

Relevant academic research and scientific papers

Total synthesis of malyngamides K, L, and 5″-epi-C and absolute configuration of malyngamide L

An accelerated, enantioselective, and general synthetic route to a class of malyngamides, K (1), L (3), and 5″-epi-C (4), bearing a cyclohexenone ring or a heavily oxygenated six-membered ring and a vinyl chloride structural motif was developed. The key s