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- W2781918233 abstract "Abstract Transition metal mediated C−H activation is a powerful synthetic tool for the total synthesis of complex natural products and biologically active molecules. The strategy involves mainly C−H activation, nucleophilic addition and regeneration of the catalyst. It proceeds through a C−H bond cleavage by ligand coordination to transition metal. Transition metals like Pd, Rh, Ru, Co, and Ir are the most often used catalysts, which form a complex with 2‐aryl pyridine and facilitates the functionalization of various C−H bonds to generate diverse C−C and C−X bonds under typically mild reaction conditions with low catalyst loading. In particular, the chelation‐assisted cleavage of C−H bonds at ortho ‐position of the pyridine directing group has been recognized as one of the most powerful strategies for the functionalization of unreactive C−H bonds. Recently, transition metal catalyzed C−H bond activation has received significant interest because it does not require the prefunctionalization of the substrate. Therefore, the metal‐catalyzed C−H activation and functionalization is currently considered as atom economy and simplified procedure in comparison with the traditional strategies." @default.
- W2781918233 created "2018-01-12" @default.
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- W2781918233 creator A5036880757 @default.
- W2781918233 creator A5068154195 @default.
- W2781918233 creator A5090608728 @default.
- W2781918233 date "2018-01-02" @default.
- W2781918233 modified "2023-10-17" @default.
- W2781918233 title "Substrate-Directed C-H Functionalization of 2-Aryl Pyridines by Transition Metal Complexes" @default.
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