64648-56-2

Upstream product

• 1146137-38-3 N-(4-methoxyphenyl)-N-methyl-2-phenylpropanamide 
• 2912-62-1 α-chlorophenylacetyl chloride 
• 150-75-4 N-methyl-p-aminophenol 
• 220580-90-5 4-hydroxy-N-methyl-N-(α-chloro-α-phenylacetyl)aniline 

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).

Syntheses and biological evaluation of (±)-3a-phenyl congeners of physostigmine and phenserine

(±)-3a-Phenyl congeners of physostigmine and phenserine, synthesized for the first time by a modification of the Julian total synthesis of physostigmine, were evaluated for anticholinesterase action against human acetyl- and butyrylcholinesterase. These a