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Improved palladium-catalyzed coupling reactions of aryl halides using

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dc.contributor.author Gurbuz, N
dc.contributor.author Ozdemir, I
dc.contributor.author Demir, S
dc.contributor.author Cetinkaya, B
dc.date.accessioned 2022-10-19T12:13:18Z
dc.date.available 2022-10-19T12:13:18Z
dc.date.issued 2004
dc.identifier.uri http://hdl.handle.net/11616/84063
dc.description.abstract The incorporation of saturated N-heterocyclic carbenes into palladium pre-catalysts gives high catalyst activity in the Suzuki coupling of aryl iodides, bromides and deactivated aryl chloride substrates, whereas the yield of the palladium catalyzed Heck reaction of deactivated aryl chlorides is negligible. The complexes were generated in the presence of Pd(OAc)(2) by in situ deprotonation of 1,3-dialkylimidazolinium salts LHX (1) which were characterized by conventional spectroscopic methods and elemental analyses. (C) 2003 Elsevier B.V. All rights reserved.
dc.description.abstract C1 Ege Univ, Dept Chem, TR-35100 Bornova, Turkey.
dc.description.abstract Inonu Univ, Dept Chem, TR-44069 Malatya, Turkey.
dc.source JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
dc.title Improved palladium-catalyzed coupling reactions of aryl halides using
dc.title saturated N-heterocarbene ligands


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