208336-26-9

Upstream product

• 56169-11-0 (-)-α-phellandrene 

Downstream Products

• 5502-76-1 2-(4-methylcyclohexyl)propan-1-ol 
• 132438-03-0 (1S,3R,4R,8S)-3,9-epoxy-p-menthane 
• 1340481-31-3 (1S,4R,8R)-3-oxo-p-menthan-9-oic acid 
• 1340481-32-4 (1S,4R,8R)-3-oxo-p-menthan-9-oic acid methyl ester 
• 1157861-49-8 (1S,4R,8S)-3-oxo-p-menthan-9-oic acid 
• 1340481-36-8 (1S,4R,8S)-3-oxo-p-menthan-9-oic acid methyl ester 
• 676248-66-1 (1R,4S,8S)-3-oxo-p-menthan-9-oic acid 
• 676248-65-0 (1R,4R,8S)-3-oxo-p-menthan-9-oic acid 
• 79726-52-6 (1R,4S,8S)-3-oxo-p-menthan-9-oic acid methyl ester 
• 1340481-23-3 (4S,8R)-p-mentha-1,5-dien-9-ol 
• 1340481-24-4 (4S,8S)-p-mentha-1,5-dien-9-yl acetate 
• 208336-25-8 2-((S)-4-Methyl-cyclohexa-2,4-dienyl)-propionic acid 
• 208336-30-5 2-((S)-4-Methyl-cyclohexa-2,4-dienyl)-propionaldehyde 

Relevant academic research and scientific papers

Enantiocontrolled formal total synthesis of paeonilactone A and B from (S)-(+)-carvone

A synthesis of enantiomerically pure lactone 11a from commercially available (S)-(+)-carvone has been developed. The synthesis constitutes a formal synthesis of paeonilactone A and B and involves a stereoselective palladium-catalyzed 1,4-oxylactonization