7287-73-2Relevant articles and documents
A green and mild procedure to selective synthesis of diarylamine via domino reaction of aryl halides and arginine catalyzed by magnetic-MOF
Soleiman-Beigi, Mohammad,Mohammadi, Fariba
, (2018)
Efficient and selective direct synthesis of diarylamines from aryl halides and arginine as a nitrogen-donor reagent is reported. Arginine, which is an oral supplement, acts as a useful nitrogen source donor in the copper-catalyzed reaction. Fe3O4/Cu3(BTC)2, which was easily separated and recycled with a magnet, improved the rate and facilitation of the synthesis of diarylamines selectively. The introduction of a new and available N-source, simple magnetic separation process, normal atmospheric conditions, and excellent yields under mild reaction conditions are other important features of this work.
Efficient copper-catalyzed coupling of aryl chlorides, bromides and iodides with aqueous ammonia
Xu, Hanhui,Wolf, Christian
scheme or table, p. 3035 - 3037 (2009/12/01)
The copper(i)-catalyzed synthesis of a range of primary anilines from electron-rich and electron-deficient aryl halides including aryl chlorides has been achieved with aqueous ammonia, avoiding the need for inert atmosphere, expensive catalysts and ligands, anhydrous solvents, and additional base or other additives. The Royal Society of Chemistry 2009.
Phase-Transfer Catalysis in the Ullmann Synthesis of Substituted Triphenylamines
Gauthier, Sylvie,Frechet, Jean M. J.
, p. 383 - 385 (2007/10/02)
A variety of substituted triphenylamine derivatives were prepared in nearly quantitative yields by the use of 18-crown-6 as a phase transfer catalyst under the Ullmann reaction conditions.
