90986-71-3

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 320369-29-7 N′-(1-([1,1′-biphenyl]-4-yl)ethylidene)-4-methylbenzenesulfonohydrazide 
• 92-91-1 biphenyl-4-acetaldehyde 
• 13392-79-5 1-chloro-4-(1-(4-methoxyphenyl)vinyl)benzene 
• 98-80-6 phenylboronic acid 
• 637-87-6 1-Chloro-4-iodobenzene 
• 32117-52-5 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine 
• 100-07-2 4-methoxy-benzoyl chloride 
• 92-52-4 biphenyl 
• 917-64-6 methyl magnesium iodide 
• 79447-11-3 [1,1'-biphenyl]-4-yl(4-methoxyphenyl)methanone 
• 3315-91-1 4-biphenylylmagnesium bromide 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

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

Syntheses of Asymmetrical Diaryl and Aryl Alkyl Ketones as Possible Non-steroidal Antiprogestational Agents

A number of asymmetrical diaryl and aryl alkyl ketones have been synthesised as possible non-steroidal antiprogestational agents.Evaluation of these compounds as competitive inhibitors of progesterone binding to uterine cytosol progesterone receptors of rabbit and human indicates that 3-methyl-4'-phenylbenzophenone (2) exhibits marginal activity in both the cases.However, this compound has been found to be inferior to R 5020 and d-norgestrel.