55210-79-2

Upstream product

• 86-52-2 1-Chloromethylnaphthalene 
• 133745-75-2 N-fluorobis(benzenesulfon)imide 

Downstream Products

• 55210-82-7 4-naphthalen-1-ylmethyl-N,N'-diphenyl-[1,2,4]dithiazolidine-3,5-diylidenediamine 
• 1093682-84-8 1-(naphthalen-1-ylmethyl)aziridine-2-(N-phenyl)carboxamide 
• 1093682-85-9 1-(naphthalen-1-ylmethyl)aziridine-2-(N-cyclohexyl)carboxamide 
• 118-31-0 (naphth-1-yl)methylamine 
• 86-53-3 1-Cyanonaphthalene 
• 1309877-93-7 C₇₇H₁₁₃N₁₅O₁₄ 
• 32280-54-9 N-(naphthalen-1-ylmethyl)benzamide 
• 1602731-60-1 C₂₆H₂₁N₅O 
• 1602732-83-1 C₂₆H₂₁N₅O 
• 66-77-3 1-naphthaldehyde 
• 16413-71-1 N,N-dimethyl(naphthalen-1-yl)methanamine 
• 14489-75-9 N-methyl-1-naphthalenemethylamine 
• 95048-05-8 1-naphthaldimine 

Relevant academic research and scientific papers

An efficient transformation of primary halides into nitriles through palladium-catalyzed hydrogen transfer reaction

Two-step one-pot transformation of primary halides into corresponding nitriles is successfully achieved. Nucleophilic substitution of primary halides with sodium azide and subsequent palladium-catalyzed hydrogen transfer proceeds smoothly in the presence of sterically bulky ligand dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (XPhos) in acetone to produce nitriles in satisfactory to good yields. This journal is

Palladium-Catalyzed Intermolecular Oxidative Diazidation of Alkenes

A palladium-catalyzed oxidative vicinal diazidation of alkenes has been developed, in which TMSN3 was used as azide source. Both styrenes and unactivated alkenes are suitable for this reaction. And trans-alkyldiazides were obtained as major products from cyclic alkenes with moderate to good diastereoselectivities. This reaction afforded an efficient way for the synthesis of useful 1,2-diamines after hydrogenation.