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- W2969363058 endingPage "120906" @default.
- W2969363058 startingPage "120906" @default.
- W2969363058 abstract "In the present study, synthesis and catalytic properties of palladium PEPPSI type complexes of cycloheptyl substituted N-heterocyclic carbene ligand were reported. Different N-coordinate ligands including pyridine, imidazole and thiazole derivatives were used to stabilize the complexes. Structures of complexes were established by 1H NMR, 13C NMR, IR spectroscopic methods and elemental analyses. All complexes were applied to Suzuki-Miyaura cross coupling reaction in aqueous media. After the optimization of reaction conditions, all complexes were tested on the cross coupling of five different aryl chloride derivatives and phenylboronic acid. Pyridine containing complex, 3a performed stronger catalytic performance than others." @default.
- W2969363058 created "2019-08-29" @default.
- W2969363058 creator A5058012512 @default.
- W2969363058 date "2019-10-01" @default.
- W2969363058 modified "2023-09-28" @default.
- W2969363058 title "Cycloheptyl substituted N-heterocyclic carbene PEPPSI-type palladium complexes with different N-coordinated ligands: Involvement in Suzuki-Miyaura reaction" @default.
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- W2969363058 doi "https://doi.org/10.1016/j.jorganchem.2019.120906" @default.
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