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Cross coupling reactions catalyzed by (NHC)Pd(II) complexes

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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. |

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Synthesis, characterization, and microwave-assisted catalytic activity in Heck, Suzuki, Sonogashira, and Buchwald–Hartwig cross-coupling reactions of novel benzimidazole salts bearing N-phthalimidoethyl and benzyl moieties

Substituted 2-(2’-pyridyl)benzimidazole palladium(II) complexes as an efficient catalytic system for Suzuki–Miyaura cross-coupling reactions

Contribution of heterobifunctional ligands to transition metal-catalysed C–C coupling reactions

Planar Geometry of 4-Substituted-2,2'-bipyridines Synthesized by Sonogashira and Suzuki Cross-Coupling Reactions

Programmed Synthesis of Tetraarylthieno[3,2-b]thiophene by Site-Selective Suzuki Cross-Coupling Reactions of Tetrabromothieno[3,2-b]thiophene

Density functional theory-supported studies of structural and electronic properties of substituted-phenol derivatives synthesized by efficient O- or C-arylation via Chan–Lam or Suzuki cross-coupling reactions

New Pd(II) and Pt(II)-diaminophosphine complexes bearing cyclohexyl or isopropyl moiety: use of Pd(II) complexes as precatalyst in Mizoroki–Heck and Suzuki–Miyaura cross-coupling reactions

Planar Geometry of 4-Substituted-2,2'-bipyridines Synthesized by Sonogashira and Suzuki Cross-Coupling Reactions

Cross coupling reactions catalyzed by (NHC)Pd(II) complexes

Heck reactions of aryl halides with styrene using 1-butyl-3-methylimidazolium bromide ionic liquid as a green solvent under microwave irradiation

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