85937-47-9

Upstream product

• 85937-48-0 N-Methyl-2-phenylbutyrthioanilid 
• 36854-57-6 2-Phenylbutyryl chloride 
• 100-61-8 N-methylaniline 

Downstream Products

• 85937-46-8 2-ethyl-3-(N-methyl-N-phenylamino)-2-phenyl-2H-azirine 
• 85937-51-5 N¹-Methyl-N¹-phenyl-N²-(1'-phenyl-1'-propenyl)formamidin 
• 35524-76-6 N-(2-fluorophenyl)-N-methylcyclohexanecarboxamide 

Relevant academic research and scientific papers

Oxindole synthesis by direct coupling of Csp2-H and C sp3-H centers

(Chemical Equation Presented) An sp2/sp3 get-together: A novel and efficient method can be used to synthesize 3,3-disubstitued oxindoles by the direct intramolecular oxidative coupling of an aryl Csp2-H and a Csp3-H center (see scheme; DMF = N,N-dimethylformamide).

Photochemically Induced Reactions of 3-Amino-2H-azirines

Irradiation of 3-(N-methylanilino)-2H-azirines with a mercury low pressure lamp induces the cleavage of the C(2), C(3)-ring bond thus affording nitriliomethanide dipols, substituted by an amino group at C(1).Depending on the substitution pattern at C(3),