Abstract
Amination and amidation of aryl compounds using a transition-metal-catalyzed cross-coupling reaction typically involves prefunctionalization or preoxidation of either partner. In recent years, a new class of transition-metal-catalyzed cross-dehydrogenative coupling reaction has been developed for the direct formation of aryl C-N bonds. This short review highlights the substantial progress made for ortho -C-N bond formation via transition-metal-catalyzed chelation-directed aryl C-H activation and gives an overview of the challenges that remain for directed meta - and para -selective reactions. 1 Introduction 2 Intramolecular C-N Cross-Dehydrogenative Coupling 2.1 Nitrogen Functionality as Both Coupling Partner and Directing Group 2.2 Chelating-Group-Directed Intramolecular C-N Bond Formation 3 Intermolecular C-N Cross-Dehydrogenative Coupling 3.1 ortho -C-N Bond Formation 3.1.1 Copper-Catalyzed Reactions 3.1.2 Other Transition-Metal-Catalyzed Reactions 3.2 meta - and para -C-N Bond Formation 4 C-N Cross-Dehydrogenative Coupling of Acidic C-H Bonds 5 Conclusions.
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Henry, M. C., Mostafa, M. A. B., & Sutherland, A. (2017, October 17). Recent Advances in Transition-Metal-Catalyzed, Directed Aryl C-H/N-H Cross-Coupling Reactions. Synthesis (Germany). Georg Thieme Verlag. https://doi.org/10.1055/s-0036-1588536
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