140710-01-6

Upstream product

• 94348-75-1 4-acetoxy-3-methylene-4-phenylbutan-2-one 
• 66680-86-2 isobutenyltributyltin 
• 150016-65-2 (3Z)-3-iodo-4-phenylbut-3-en-2-one 

Downstream Products

• 1516887-71-0 C₂₀H₂₀N₂ 

Relevant academic research and scientific papers

Regioselective synthesis of 1,3,4,5-Tetrasubstituted Pyrazoles from α-Alkenyl-α,β-Enones derived from Morita-Baylis-Hillman adducts

Convenient synthetic method for 4-arylethylpyrazoles and 4-styrylpyrazoles was developed using α-alkenyl- α,β-enones readily accessed from the Morita-Baylis-Hillman reaction. For the synthesis of 4-arylethylpyrazole, the reactions with arylhydrazines need

Modified stille coupling utilizing α-iodoenones

α-Iodoenones undergo Pd-catalyzed coupling with alkenyl- and aryltributylstannanes providing an efficient route to the corresponding α-substituted enones.