31006-89-0

Upstream product

• 71491-49-1 3-(4-Chloro-phenyl)-2,3-dimethyl-butan-2-ol 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 637-87-6 1-Chloro-4-iodobenzene 
• 62460-98-4 N′-(3,3-dimethylbutan-2-ylidene)-4-methylbenzenesulfonohydrazide 
• 30314-42-2 1-(4-chlorophenyl)-2,2-dimethylpropan-1-one 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 623-03-0 4-Cyanochlorobenzene 
• 51833-36-4 4-chlorophenylmagnesium chloride 
• 57169-53-6 1-(4-chlorophenyl)-2,2-dichloro-1-propanone 

Relevant academic research and scientific papers

Palladium-Catalyzed One-Pot Reaction of Hydrazones, Dihaloarenes, and Organoboron Reagents: Synthesis and Cytotoxic Activity of 1,1-Diarylethylene Derivatives

A new three-component assembly reaction between N-tosylhydrazones, dihalogenated arenes, and boronic acids or boronate esters was developed, producing highly substituted 1,1-diarylethylenes in good yields. The two C-C bonds formed through this coupling ha

Synergistic interplay of a non-heme iron catalyst and amino acid coligands in H2O2 activation for asymmetric epoxidation of α-alkyl-substituted styrenes

Highly enantioselective epoxidation of α-substituted styrenes with aqueous H2O2 is described by using a chiral iron complex as the catalyst and N-protected amino acids (AAs) as coligands. The amino acids synergistically cooperate with the iron center in promoting an efficient activation of H2O2 to catalyze epoxidation of this challenging class of substrates with good yields and stereoselectivities (up to 97% ee) in short reaction times.