132058-86-7

Upstream product

• 94623-43-5 N-(2-Methoxybenzoyl)-diphenylamine 
• 4357-57-7 9-bromoacridine 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 1207-69-8 9-Chloroacridine 
• 21615-34-9 2-Methoxybenzoyl chloride 
• 122-39-4 diphenylamine 
• 108350-92-1 N-(2-Iodobenzoyl)-diphenylamine 
• 1522-69-6 N-(3,4-Dimethoxybenzoyl)-diphenylamine 
• 16034-40-5 N-(4-Methoxybenzoyl)-diphenylamine 
• 73333-82-1 N-(3-Nitrobenzoyl)-diphenylamine 

Relevant academic research and scientific papers

A magnetic nanoparticle-supported N-heterocyclic carbene-palladacycle: An efficient and recyclable solid molecular catalyst for Suzuki-Miyaura cross-coupling of 9-chloroacridine

A robust magnetic nanoparticle-supported N-heterocyclic carbene-palladacycle has been readily synthesized by directly anchoring the structural defined acenaphthoimidazolylidene palladacycle with a long tail on magnetic nanoparticles (MNPs), and functioned as a solid molecular catalyst and exhibited extremely high catalytic activity towards the challenging Suzuki-Miyaura cross-coupling reactions between less-studied heterocyclic 9-chloroacridine and diverse boronic acids. Remarkably, the catalyst could be used 5 times without obvious loss of activity highlighting the efficiency of our strategy of immobilization of previledged catalysts.

Structural studies on bioactive compounds. Part 33. Synthesis of 9- arylacridines by palladium-mediated couplings

9-Halogenoacridines undergo Suzuki cross-coupling reactions with a range of arylboronic and thienyl-3-boronic acids to yield substituted 9- arylacridines and 9-(thien-3-yl)acridines.

STUDIES ON ENAMIDES. PART 4 : PHOTOCHEMICAL INVESTIGATIONS OF N-AROYLDIPHENYLAMINES

Photolysis of N-aroyldiphenylamines affords 9-arylacridines or phenanthridinone depending on the structure of the substrates.Additionally, carbazole and photomigrated products are also obtained.