37985-01-6

Upstream product

• 15175-54-9 N,N-dimethyl-4-methoxylbenzylamine 
• 1416982-07-4 1-(4-methoxyphenyl)-N,N,N-trimethylmethanaminium trifluoromethanesulfonate 
• 63888-20-0 3-phenyl-1-propen-1-yl acetate 
• 141694-63-5 (E)-1-iodo-3-phenyl-1-propene 
• 22145-08-0 (E,E)-1-(4-methoxyphenyl)-4-phenyl-1,3-butadiene 

Downstream Products

• 150660-28-9 (E)-1-methoxy-4-(4-phenylbut-1-en-1-yl)benzene 

Relevant academic research and scientific papers

Reductive Coupling between C-N and C-O Electrophiles

The cross-electrophile reaction is a promising strategy for C-C bond formation. Recent studies have focused mainly on reactions with organic halides. Here we report a coupling reaction between C-N and C-O electrophiles that demonstrates the possibility of constructing a C-C bond via C-N and C-O cleavage. Several reactions between benzyl/aryl ammonium salts and vinyl/aryl C-O electrophiles have been studied. Preliminary mechanistic studies revealed that the benzyl ammoniums were activated through a radical mechanism.

Cross-Coupling Reactions of Alkenyl Halides with 4-Benzyl-1,4- Dihydropyridines Associated with E to Z Isomerization under Nickel and Photoredox Catalysis

Cross-coupling reactions of alkenyl halides with 4-alkyl-1,4-dihydropyridines as alkylation reagents have been achieved by combination of nickel and photoredox catalysts. Alkenyl halides bearing alkyl and aryl substituents are available. Particularly, in