1416727-72-4

Upstream product

• 1609468-92-9 C₂₀H₂₄FNO₄ 
• 783-08-4 [4-(benzylideneamino)phenyl]methanol 
• 347-91-1 2-(4-fluorophenyl)-1-phenylethanone 
• 1416727-93-9 N-(2-(4-fluorophenyl)-1-phenylethylidene)-4-methoxyaniline 

Relevant academic research and scientific papers

Radical alkylation of imines with 4-alkyl-1,4-dihydropyridines enabled by photoredox/br?nsted acid cocatalysis

Radical alkylation of imines with 4-alkyl-1,4-dihydropyridines cocatalyzed by iridium/ruthenium complex and Br?nsted acid under visible light irradiation has been achieved. Both aldimines and ketimines can undergo this transformation. Common functional groups, such as hydroxyl groups, ester, amide, ether, cyanide, and heterocycles, can be tolerated in this reaction. A variety of structurally diverse amines (57 examples) have been produced with up to 98% isolated yields using this method.

Highly enantioselective hydrosilylation of N-(1,2-diarylethylidene) arylamines

By employing a chiral Lewis base as the catalyst, enantioselective hydrosilylation of N-(1,2-diarylethylidene)arylamines was realized. The reactions proceeded smoothly to afford various chiral 1,2-diarylethanamines with good yields (up to 99%) in good ena