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Showing papers by "Nevin Gürbüz published in 2016"


Journal ArticleDOI
TL;DR: In this article, new benzimidazolium sulfonate salts have been prepared and fully characterized and they have been associated in situ with [RuCl2(p-cymene)]2 to generate efficient catalytic systems operating at 120 °C under neat conditions in the presence of potassium tert-butylate for selective N-alkylation of primary aromatic amines into secondary amines.

33 citations


Journal ArticleDOI
TL;DR: In this paper, Ag-N-heterocyclic carbene complexes were used as transmetallation reagents for the synthesis of Pd-Nhetercycleclic carbenes, and the crystal structure of one, namely dichlorobis[1,3-bis(2-methylbenzyl)imidazolidin-2-yliden]palladium(II), is presented.
Abstract: N-Aryl amination and the Buchwald–Hartwig reaction are of great synthetic and industrial interest and scientists accept their usefulness and versatility for obtaining arylamines. In this study Ag–N-heterocyclic carbene complexes were used as transmetallation reagents for the synthesis of Pd–N-heterocyclic carbene complexes. The new Pd–N-heterocyclic carbene complexes were characterized using elemental analysis and 1H NMR, 13C NMR and infrared spectroscopies. The crystal structure of one, namely dichlorobis[1,3-bis(2-methylbenzyl)imidazolidin-2-yliden]palladium(II), is presented. The activity of the Pd(II) complexes in the coupling reaction of anilines or amines with bromobenzene was investigated. These complexes exhibited high catalytic activities in the direct synthesis of triarylamines and secondary amines in a single step. Copyright © 2016 John Wiley & Sons, Ltd.

4 citations


Journal ArticleDOI
TL;DR: In this article, a review of new developments reported during the last three years concerning the catalytic performances of in situ formed or preformed NHC-Pd(II) complexes (NHC: $N$-heterocyclic carbene) for cross-coupling reactions such as Heck--Mizoraki (often shortened to the Heck reaction), Kumada, Negishi, Suzuki--Miyaura (often shorten to the Suzuki reaction), Sonogashira and Hiyama couplings, and Buchwald--Hartwig aminations, which are
Abstract: This review is focused on new developments reported during the last 3 years concerning the catalytic performances of in situ formed or preformed NHC--Pd(II) complexes (NHC: $N$-heterocyclic carbene) for cross-coupling reactions such as Heck--Mizoraki (often shortened to the Heck reaction), Kumada, Negishi, Suzuki--Miyaura (often shortened to the Suzuki reaction), Sonogashira and Hiyama couplings, and the Buchwald--Hartwig aminations, which are extremely powerful in the formation of C--C and C--heteroatom bonds. Due to the great number of publications and limited space here, we made a special attempt to compile the relevant data in tables, which we hope will serve as a guide for chemists interested in these reactions. The syntheses of the precatalysts and the generally accepted reaction mechanisms are also briefly described.