[ASAP] Speciation and Reactivity of Mono- and Binuclear Ni Intermediates in Aminoquinoline-Directed C–H Arylation and Benzylation

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This article focuses on the speciation and reactivity of mono- and binuclear nickel intermediates in aminoquinoline-directed C-H arylation and benzylation reactions. It likely discusses the mechanism of these reactions, the formation of different nickel intermediates, and their role in the overall process. Understanding these intermediates is crucial for improving the efficiency and selectivity of these transformations, which can have implications for the development of new synthetic methodologies in organic chemistry.

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