Recent approaches for the synthesis of heterocycles from amidines via a metal catalyzed C–H functionalization reaction

Abstract

Transition metal catalyzed C–H bond activation has become one of the most important tools for constructing new chemical bonds. Introducing directing groups to the substrates is the key to a successful reaction, these directing groups can also be further transformed in the reaction. Amidines with their unique structure and reactivity are ideal substrates for transition metal-catalyzed C–H transformations. This review describes the major advances and mechanistic investigations of the C–H activation/annulation tandem reactions of amidines until early 2024, focusing on metal-catalyzed C–H activation of amidines with unsaturated compounds, such as alkynes, ketone, vinylene carbonate, cyclopropanols and their derivatives. Meanwhile this manuscript also explores the reaction of amidines with different carbene precursors, for example diazo compounds, azide, triazoles, pyriodotriazoles, and sulfoxonium ylides as well as their own C–H bond activation/cyclization reactions. A bright outlook is provided at the end of the manuscript.