861219-72-9

Upstream product

• 159682-69-6 3-(but-3-enyl)-3-ethylpiperidin-2-one 
• 159682-46-9 3-(but-3-ynyl)-3-ethylpiperidin-2-one 
• 155193-60-5 3-(Buten-4-yl)-2(1H)-piperidinone 
• 675-20-7 piperidin-2-one 
• 861219-78-5 3-[4-(2-aminophenyl)-but-3-ynyl]-3-ethyl-piperidin-2-one 
• 861219-79-6 3-[(Z)-4-(2-Amino-phenyl)-but-3-enyl]-3-ethyl-piperidin-2-one 
• 861219-80-9 [2-[(Z)-4-(3-ethyl-2-oxopiperidin-3-yl)but-1-enyl]phenyl]carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Application of cross-conjugated heteroaromatic betaines to the synthesis of the schizozygane alkaloid (±)-strempeliopine

(Chemical Equation Presented) An efficient stereocontrolled route to the isoschizozygane alkaloid core has been developed utilizing an intramolecular 1,4-dipolar cycloaddition of a cross-conjugated heteroaromatic betaine. The resulting cycloadduct undergo

An approach to the isoschizozygane alkaloid core using a 1,4-dipolar cycloaddition of a cross-conjugated heteroaromatic betaine

(Chemical Equation Presented) A new strategy for the synthesis of the isoschizozygane alkaloid core has been developed that is based on a 1,4-dipolar cycloaddition reaction of a cross-conjugated heteroaromatic betaine. The resulting cycloadduct undergoes