444990-74-3

Upstream product

• 1027791-42-9 (1S,5S)-5-Isopropenyl-1,2,6,6-tetramethyl-cyclohex-2-enol 
• 179259-37-1 (+)-(5S)-5-isopropenyl-2,6,6-trimethylcyclohex-2-enone 
• 302840-38-6 (+)-(5S)-5-isopropenyl-2,3,4,4-tetramethylcyclohex-2-en-1-one 

Downstream Products

• 444990-86-7 (-)-2-[(1S,5S)-5-isopropenyl-1,2,6,6-tetramethylcyclohex-2-enyl]acetic acid 
• 874201-07-7 1-Diazo-3-((1S,5S)-5-isopropenyl-1,2,6,6-tetramethyl-cyclohex-2-enyl)-propan-2-one 
• 444990-75-4 (-)-ethyl 2-[(1S,5S)-5-isopropenyl-1,2,6,6-tetramethylcyclohex-2-enyl]acetate 
• 221664-35-3 ((1S,5S)-5-Isopropenyl-1,2,6,6-tetramethyl-cyclohex-2-enyl)-acetaldehyde 

Relevant academic research and scientific papers

An enantiospecific approach to (+)-thaps-8(11)-en-3-ol

An enantiospecific synthesis of a thapsane containing an oxygen substituent at the C-3 position is accomplished starting from (R)-carvone. A Claisen rearrangement and an intramolecular diazoketone cyclopropanation reaction were employed for the stereo- an

Enantiospecific synthesis of sesquiterpenes from (R)-carvone. Synthesis of 3-thapsenol

Enantiospecific synthesis of 3-thapsenol, comprising the carbon framework of a small group of sesquiterpenes containing three contiguous quaternary carbon atoms has been described. (R)-Carvone has been employed as the chiral starting material utilizing th

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.