179259-35-9

Upstream product

• 179259-32-6 (+)-(1S,5R)-3-allyl-2-methyl-5-isopropenylcyclohex-2-enyl acetate 
• 6485-40-1 (R)-Carvone 
• 179259-34-8 (+)-(1S,5R)-3-allyl-2-methyl-5-isopropenylcyclohex-2-enol 
• 179259-33-7 (+)-(5S)-3-allyl-2-methyl-5-isopropenylcyclohex-2-enone 
• 227000-91-1 (R)-1-Allyl-5-isopropenyl-2-methyl-cyclohex-2-enol 
• 179465-41-9 (1R,5R)-1-Allyl-5-isopropenyl-2-methyl-cyclohex-2-enol 

Relevant academic research and scientific papers

Model Studies Directed Towards the Synthesis of Functionalised Chiral A-ring Derivatives of Taxanes

Model studies, starting from the monoterpene R-carvone, directed towards the synthesis of chiral A-ring derivatives of taxanes with oxygen functionalities at C-2,9 and 13 carbon atoms as in taxol is described.

Synthesis of taxanes - The carvone approach; a simple, efficient stereo- and enantio-selective synthesis of the functionalised A ring

A highly stereo- and enantio-selective methodology for the construction of the chiral functionalised A-ring of taxanes, starting from (R)-carvone employing a short, simple and efficient sequence is described.