145801-91-8

Upstream product

• 36394-07-7 5-hexenoyl chloride 
• 889-31-6 5,5-dimethyl-3-benzylamino-2-cyclohexen-1-one 
• 100-46-9 benzylamine 
• 3471-13-4 dimedone 
• 145801-85-0 N-benzyl-N-(5,5-dimethyl-3-oxocyclohex-1-enyl)hex-5-enamide 

Relevant academic research and scientific papers

Intramolecular [2 + 2] photocvcloaddition of N-alkenovl-β-enaminones

The photolysis of cyclic N-alkenoyl β-enaminones is described. In general, a very regio- and stereoselective intramolecular [2 + 2] photocydoaddition was observed. The limitations of the reaction process are discussed. The main competitive reaction, which

Intramolecular [2+2] photocycloaddition of N-alkenoyl β - enaminones

Intramolecular cycloaddition of N-alkenoyl β-enaminones occurs with high regioselectivity and diastereoselectivity leading to interesting synthons for the total synthesis of triquinanes or various sesquiterpenes.