N, N-Dimethylaniline and N, N-diethylaniline react with Cu2+ to form the corresponding
amine radical cations. The radical cations were characterized by their absorption spectra. In …

Microwave-assisted synthesis of 4,4′-diaminotriphenylmethanes - ScienceDirect Skip to main
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Remarkably efficient oxidative coupling of N,N-dialkylarylamines in water mediated by
cerium(IV) ammonium nitrate - ScienceDirect Skip to main contentSkip to article Elsevier …

Naphthalene-1, 8-diylbis (diphenylmethylium) exhibits a unique electron-transfer reduction
behavior due to the close proximity of the two triarylmethyl cations, which form a C− C bond …

Utilization of dioxygen as the terminal oxidant at ambient temperature is always a challenge
in redox chemistry, because it is hard to oxidize a stable redox metal ion like iron (III) to its …

Biaryl diamines are important building blocks in organic synthesis. Consequently, it is
desirable to develop a general and mild synthetic approach to diverse biaryl diamines …

An efficient, versatile and solvent‐free synthetic technique of diaminotriarylmethanes was
reached by treating N, N‐dimethylaniline with some arylaldehydes over zirconium (IV) oxide …

A new and efficient protocol to prepare 2-(R-anilino)-1, 4-naphthoquinones in quantitative
yields is presented. This synthesis occurs under mild conditions by reacting the …

Full article: Oxidative Coupling Reaction of N,N‐Dialkylanilines with Cerium(IV) Ammonium
Nitrate in the Solid State Skip to Main Content Taylor and Francis Online homepage Browse …

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