120238-18-8

Upstream product

• 120238-17-7 3-cyano-3-(3-methoxyphenyl)propanenitrile 
• 541-59-3 maleiimide 
• 10365-98-7 3-methoxyphenylboronic acid 
• 24393-44-0 2-cyano-3-(3-methoxyphenyl)acrylic acid ethyl ester 
• 591-31-1 3-methoxy-benzaldehyde 

Downstream Products

• 38913-02-9 3-(3-methoxyphenyl)-1-(methyl)pyrrolidine-2,5-dione 
• 143883-83-4 1-Butyl-3-(3-methoxy-phenyl)-pyrrolidine 
• 144076-27-7 3-(1-Butyl-pyrrolidin-3-yl)-phenol; hydrobromide 
• 120238-27-9 1,4-dimethyl-3-(3-methoxyphenyl)-3-pyrroline-2,5-dione 
• 120238-22-4 4-ethoxalyl-3-(3-methoxyphenyl)-1-(methyl)pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

Microwave-enhanced rhodium-catalyzed conjugate-addition of aryl boronic acids to unprotected maleimides

Various boronic acids were treated with a rhodium (I) catalyst enabling their 1,4-conjugate addition to unprotected maleimide. The scope of the reaction was explored to include both electron-rich and electron poor boronic acids. These reactions were also

Synthesis of cis-4-methyl-3-phenylpyrrolidines as potential dopaminergic agonists

cis-3-(3,4-Dihydroxyphenyl)-4-methyl-l-(n-propyl)pyrrolidine (23) was synthesized and evaluated for dopaminergic activity. The synthesis of 23 involved selective 4-acylation of the 3-phenylpyrrolidine-2,5-dione 15 and cis-addition of hydrogen to a 4-methy