221664-47-7

Upstream product

• 766-04-1 benzyllithium 
• 6485-40-1 (R)-Carvone 
• 100-39-0 benzyl bromide 
• 852930-24-6 (1S,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enol 
• 483305-68-6 3-benzyl-carvone 

Downstream Products

• 221664-51-3 ((1R,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-acetaldehyde 
• 863725-59-1 Benzoic acid (1R,5S)-3-benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl ester 
• 221664-59-1 (1R,6R)-1-Benzyl-9-methyl-5-methylene-bicyclo[4.3.1]dec-8-en-3-one 
• 863725-51-3 ((1R,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-acetic acid ethyl ester 
• 863725-61-5 ((1S,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-acetic acid ethyl ester 
• 863725-52-4 ((1R,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-acetic acid 
• 863725-62-6 ((1S,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-acetic acid 
• 863725-53-5 1-((1R,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-3-diazo-propan-2-one 
• 863725-63-7 1-((1S,5R)-1-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enyl)-3-diazo-propan-2-one 
• 863725-60-4 (1R,5S)-3-Benzyl-5-isopropenyl-2-methyl-cyclohex-2-enol 

Relevant academic research and scientific papers

Stereo- and regioselective construction of vicinal stereogenic quaternary carbon atoms: Enantiospecific approach to cyperanes

An enantiospecific approach to a functionalised carbon framework of the sesquiterpenes, cyperanes, starting from the monoterpene (R)-carvone has been accomplished. A combination of a Claisen rearrangement, intramolecular diazo ketone cyclopropanation and

Synthesis of chiral bicyclo[4.3.1]decanes via an intramolecular carbonyl ene-reaction

Synthesis of chiral bicyclo[4.3.1]decanes via an intramolecular acid catalysed type II ene reaction of chiral (5-isopropenylcyclohex-2- enyl)acetaldehydes derived from (R)-carvone is described.