188540-03-6

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 166022-29-3 (S)-(+)-(2',2'-dimethyl-6'-methylene-1'-cyclohexyl)methanol 
• 472-19-5 (2,2-dimethyl-6-methylenecyclohexyl)methanol 
• 166239-08-3 methyl (1S)-(+)-2,2-dimethyl-6-methylene-1-cyclohexanecarboxylate 
• 166022-22-6 (1S)-(+)-2,2-dimethyl-6-methylene-1-cyclohexanecarboxylic acid 

Downstream Products

• 924884-84-4 (S)-2,2-dimethyl-6-methylene-1-[3'-(1''-phenyl-1''H-tetrazole-5''-sulfanyl)butyl]cyclohexane 
• 924884-90-2 (S)-2,2-dimethyl-1-[3'-(benzothiazole-2''-sulfanyl)butyl]-6-methylenecyclohexane 
• 502763-37-3 (2E,6E)-9-((1S)-2,2-dimethyl-6-methylenecyclohexyl)-3,7-dimethyl-1-(tetrahydro-2-pyranyl)oxy-2,6-nonadiene 
• 145398-68-1 luffarin-P 
• 502763-33-9 (S)-(-)-2,2-dimethyl-6-methylene-1-[1'-(phenylthio)methyl]cyclohexane 
• 502763-34-0 (S)-1-[1′-benzenesulfonyl]methyl-2,2-dimehtyl-6-methylenecyclohexane 
• 473-03-0 (1R,4aα)-1-[(E)-6-[(S)-2,2-dimethyl-6-methylenecyclohexyl]-4-methyl-3-hexenyl]decahydro-2,5,5,8aβ-tetramethylnaphthalene-2α-ol 
• 188559-03-7 (S)-2-Bromomethyl-1,1-dimethyl-3-methylene-cyclohexane 

Relevant academic research and scientific papers

Preparation of (S)-γ-cyclogeraniol by lipase-catalyzed transesterification and synthesis of (+)-trixagol and (+)-luffarin-P

Lipase-catalyzed kinetic resolution of γ-cyclogeraniol by Candida antarctica lipase B yielded 23% of enantiomerically pure (S)-γ-cyclogeraniol. (+)-trixagol and (+)-luffarin-P were synthesized from the obtained (S)-γ-cyclogeraniol, and the absolute config

Synthesis of (+)-Ambrein

Enantiomerically pure (+)-Ambrein was synthesized from (+)-drimane-8,11-diol prepared via lipase catalyzed kinetic resolution, and easily prepared (i)-γ-cyclogeraniol.