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Upstream product

• 848-83-9 1,3-diphenylnaphthalene 
• 881811-70-7 2,4-diphenyl-1-naphthylamine 
• 20191-76-8 2,4-dibromo-1-naphthylamine 
• 134-32-7 1-amino-naphthalene 

Downstream Products

• 848-83-9 1,3-diphenylnaphthalene 
• 881811-83-2 2,4-diphenyl-1-naphthylboronic acid 

Relevant academic research and scientific papers

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME

Provided is a compound capable of significantly improving lifespan, efficiency, electrochemical stability, and thermal stability of organic light-emitting devices. Moreover, provided is an organic light-emitting device in which the compound is contained in an organic compound layer. To this end, the compound is represented by chemical formula 1.COPYRIGHT KIPO 2018

Asymmetric Strecker reaction of aldimines using aqueous potassium cyanide by phase-transfer catalysis of chiral quaternary ammonium salts with a tetranaphthyl backbone

The phase-transfer-catalyzed, highly enantioselective cyanation of aldimines using aqueous KCN has been realized based on the molecular design of chiral quaternary ammonium iodide 2c bearing a stereochemically defined tetranaphthyl backbone. For example,

Synthesis of fused polycycles by 1,4-palladium migration chemistry

Novel palladium migration/arylation methodology for the synthesis of complex fused polycycles has been developed, in which one or more sequential Pd-catalyzed intramolecular migration processes involving C-H activation are employed. The chemistry works best with electron-rich aromatics, which is in agreement with the idea that these palladium-catalyzed C-H activation reactions parallel electrophilic aromatic substitution.