680218-19-3

Upstream product

• 680218-11-5 methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate 
• 680218-13-7 methyl 2-[2-((1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]-3-hydroxybutanoate 
• 680218-15-9 2-[2-((1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]butane-1,3-diol 
• 217467-50-0 (1S,7S)-1,8,8-trimethyl-2-oxabicyclo[5.4.0]undecan-3-one 
• 60134-39-6 (-)-(4aS,8aS)-3,4,4a,5,6,7,8,8a-octahydro-5,5,8a-trimethylnaphthalen-1(2H)-one 
• 680218-17-1 2-[2-((1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]-3-hydroxybutyl 4-methylbenzenesulfonate 

Downstream Products

• 145631-62-5 3-[2-((2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]but-3-en-2-one 

Relevant academic research and scientific papers

An Efficient Alternative Synthesis of (+)-(6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the (S)-Enantiomer of the Antibacterial Sesquiterpene from Premna oligotricha

The title compound has been synthesized from optically active lactone derived from (S)-(+)-Wieland-Miescher ketone analogue employing solid-state Baeyer-Villiger reaction.