Significant process intensification of the amination reactions of aryl halides and esters has been demonstrated using continuous flow processing. Using this technology traditionally difficult amination reactions have been performed safely at elevated temperatures. These reactions were successfully conducted on laboratory scale coil reactor modules with 1 mm internal diameter (ID) and on a prepa...

A redox amination strategy was developed for the synthesis of N-aryl-1-aminoindoles by N-N bond formation. Reaction of nitrosobenzenes with readily available indolines using Brønsted acid catalysis allows N-N bond formation under mild conditions. This method exploits the inherent reducing power of indoline to synthesize biologically relevant molecular architectures via redox amination. A one-po...

Palladium catalysed coupling reactions on haloporphyrins have revolutionised the functionalisation of the porphyrin periphery. There are now many and varied examples of successful C–C and C–X couplings, expecially on the meso positions(s) of 5,15-diarylor 5,10,15-triarylporphyrins, to produce a range of functionalised mononuclear derivatives, as well as diand oligonuclear arrays with alkynyl, a...

In present research work, homogeneous anion exchange membranes based on polysulfone (QAPSFs) were prepared via chloromethylation, amination and alkalization. In amination step, trimethylamine and N,N,N',N'-tetramethyl-1,6-hexanediamine were used as amination and crosslinking agents, respectively. The chloromethylated polysulfone was characterized by 1HNMR spectroscopy and chloromethylation degr...

A straightforward and efficient method for the synthesis of 1,2-diaryl-substituted enamines through the Cu-catalyzed electrophilic amination reaction of O-benzoyl hydroxylamines with vinylaluminum reagents generated in situ from the Ni-catalyzed hydroalumination of readily accessible internal aryl acetylenes is described. The amination is catalyzed by 1 mol% CuCl without any additive at ambient...

An improved protocol was described for the amination of chloroarenes with diarylamines under NiCl2(PCy3)2 catalysis in the presence of a Grignard reagent as base. This method fully suits bromo-/iodoarene substrates as well, and even is expanded to certain aryl tosylates. A preliminary investigation into the mechanism suggests that this amination reaction might proceed through Ni(I) and Ni(III) ...

Nitrogen-doped activated carbons with high surface areas obtained from resorcinol and formaldehyde resins were evaluated as CO2 adsorbents in a simulated flue gas stream under anhydrous and humid conditions. These carbons were prepared using two approaches, namely ammonia treatment without nitric acid pre-oxidation and amination after preoxidation. The pre-oxidation of activated carbons conside...