S
Sedat Yaşar
Researcher at İnönü University
Publications - 92
Citations - 1297
Sedat Yaşar is an academic researcher from İnönü University. The author has contributed to research in topics: Catalysis & Carbene. The author has an hindex of 18, co-authored 75 publications receiving 942 citations. Previous affiliations of Sedat Yaşar include Gaziosmanpaşa University & Cardiff University.
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Journal ArticleDOI
Synthesis and catalytic applications of palladium N-heterocyclic carbene complexes as efficient pre-catalysts for Suzuki-Miyaura and Sonogashira coupling reactions
Lamia Boubakri,Lamia Boubakri,Sedat Yaşar,Vincent Dorcet,Thierry Roisnel,Christian Bruneau,Naceur Hamdi,İsmail Özdemir +7 more
TL;DR: A new palladium complex series with N-heterocyclic carbene (NHC), pyridine and phosphine ligands, PdCl2(L)NHC (2a-c)(L = NHC), PdC2L1NHC(3a−c) NHC(L1 = Pyridine, pryidine, and triphenylphosphine) was synthesized and fully characterized in this paper.
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Ruthenium(II) N -heterocyclic Carbene Complexes in the Transfer Hydrogenation of Ketones
TL;DR: In this paper, the reduction of ketones to alcohols via transfer hydrogenation was achieved with catalytic amounts of ruthenium-N-heterocyclic carbene complexes (2−7) in the presence of t-BuOK.
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Synthesis, characterization and the Suzuki-Miyaura coupling reactions of N-heterocyclic carbene-Pd(II)-pyridine (PEPPSI) complexes
TL;DR: In this article, a new series of air and moisture-stable NHC-PdCl 2 -pyridine complexes, (2a-f ) have been described with the development of a more efficient catalytic system for the cross-coupling of aryl halides in mind.
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Transfer Hydrogenation of Ketones by Ruthenium Complexes Bearing Benzimidazol‐2‐ylidene Ligands
TL;DR: A series of benzimidazolium ligand precursors were metalated with RuCl 2 (p-cymene) 2 to give ruthenium(II) N-heterocyclic carbene complexes as mentioned in this paper.
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Benzylic Imidazolidinium, 3,4,5,6-Tetrahydropyrimidinium and Benzimidazolium Salts: Applications in Ruthenium-Catalyzed Allylic Substitution Reactions
TL;DR: In this paper, Imidazolidinium, tetrahydropyrimidinium and benzimidazolium salts were prepared in situ to produce ruthenium catalysts that are active for the substitution of allylic substrates by dimethyl malonate as a carbon nucleophile and phenol.