52612-55-2

Upstream product

• 178616-48-3 (+/-)-Ethyl 2-<2-(2,6,6-trimethyl-2-cyclohexen-1-yl)ethyl>-3-oxobutanoate 
• 154084-90-9 (+/-)-3-(2-Iodoethyl)-2,4,4-trimethyl-1-cyclohexene 
• 472-63-9 2-(2,6,6-trimethyl-cyclohex-2-enyl)-ethanol 
• 52567-91-6 (1S*,6R*)-1,7,7-Trimethyl-2-oxabicyclo<4.4.0>decan-3-one 
• 52567-55-2 3-((R)-2,6,6-Trimethyl-cyclohex-2-enyl)-propionic acid methyl ester 
• 52612-54-1 (+)-(R)-3-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-(E)-propensaeure 
• 52567-54-1 (E)-3-((R)-2,6,6-Trimethyl-cyclohex-2-enyl)-acrylic acid methyl ester 
• 24190-29-2 (R)-α-ionone 
• 52567-56-3 (-)-α-Cyclogeranylethanol 

Downstream Products

• 52567-91-6 (1S*,6R*)-1,7,7-Trimethyl-2-oxabicyclo<4.4.0>decan-3-one 

Relevant academic research and scientific papers

Synthesis of mono- and sesquiterpenoids, XXV: Synthesis of (6R*,7R*)-7-hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the racemate of the antibacterial sesquiterpene from premna oligotricha, and its (6R*,7R*) isomer

The structure of the antibacterial sesquiterpene from Premna oligotricha was shown to be not 1 but 2 (relative stereochemistry) by the unambiguous synthesis of both (±)-1 and (±)-2. VCH Verlagsgesellschaft mbH, 1996.