212626-87-4

Upstream product

• 19472-74-3 2-(2-bromophenyl)acetonitrile 
• 75-03-6 ethyl iodide 

Downstream Products

• 212626-91-0 2-(2-bromophenyl)-2-ethylbutyraldehyde 
• 13312-96-4 2-ethyl-2-phenylbut-3-enenitrile 
• 1422149-01-6 N-acetyl-2-(2-bromophenyl)-2-ethylbutanamide 
• 1422148-72-8 2-(2-bromophenyl)-2-ethylbutanamide 
• 212627-02-6 4-(2-bromophenyl)4-ethylhexanoic acid ethyl ester 
• 212626-97-6 4-(2-bromophenyl)-4-ethylhex-2-enoic acid ethyl ester 
• 929685-27-8 4-cyano-4-phenyl-hexanoic acid [2-(3,4-dimethoxy-phenyl)-ethyl]-amide 
• 929685-30-3 4-cyano-4-phenyl-hexanoic acid [2-(3,4-dimethoxy-phenyl)-ethyl]-methyl-amide 

Relevant academic research and scientific papers

Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles

An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.

Palladium-catalyzed intramolecular C(sp3)-H functionalization: Catalyst development and synthetic applications

A novel catalytic system, based on a mixture of palladium acetate and tris(5-fluoro-2-methylphenyl)-phosphane (F-TOTP), has been designed for the intramolecular C-H functionalization of alkane segments. Among other analogues of tris(2-methylphenyl)phospha