28358-70-5

Upstream product

• 92-91-1 biphenyl-4-acetaldehyde 
• 106-38-7 para-bromotoluene 
• 320369-29-7 N′-(1-([1,1′-biphenyl]-4-yl)ethylidene)-4-methylbenzenesulfonohydrazide 
• 69416-93-9 1-chloro-4-[1-(4'-methylphenyl)ethenyl]benzene 
• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 98-80-6 phenylboronic acid 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 917-64-6 methyl magnesium iodide 
• 39148-55-5 [1,1'-biphenyl]-4-yl(p-tolyl)methanone 

Relevant academic research and scientific papers

Pd(0)-Catalyzed Tandem One-Pot Reaction of Biphenyl Ketones/Aldehydes to the Corresponding Di-substituted Aryl Olefins

Synthesis of di-substituted aryl olefins via a Pd(0)-catalyzed cross-coupling reaction of biphenyl ketones/aldehydes, tosylhydrazide, and aryl bromides (or benzyl halides) was developed. This methodology was achieved by one-pot two-step reactions involvin

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