4.7 Review

Recent Advances in Metal-Catalyzed Functionalization of Indoles

期刊

ADVANCED SYNTHESIS & CATALYSIS
卷 363, 期 11, 页码 2723-2739

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.202100116

关键词

indoles; nitrogen heterocycles; C-H activation; cross-coupling; dearomatization; remote C-H activation; amination; biaryls; nickel; palladium; rhodium; phosphoric acids; transition-metal-free; Friedel-Crafts reaction

资金

  1. Rutgers University
  2. NSF [CAREER CHE-1650766]

向作者/读者索取更多资源

Indole is an important heterocycle in organic synthesis, natural products, and drug discovery, and recent research on the selective functionalization of indole has made significant advances, driven mainly by transition metal catalysis and metal-free methods. Future trends include transition-metal-catalyzed functionalization at different positions and transition-metal-free functionalization.
Indole is one of the most important heterocycles in organic synthesis, natural products, and drug discovery. Recently, tremendous advances in the selective functionalization of indoles have been reported. Although the most important advances have been powered by transition metal catalysis, exceedingly useful methods in the absence of transition metals have also been reported. In this review, we provide an overview of functionalization reactions of indoles that have been published in the last years with a focus on the most recent advances, aims, and future trends. The review is organized by the positional selectivity and type of methods used for functionalization. In particular, we discuss major advances in transition-metal-catalyzed C-H functionalization at the classical C2/C3 positions, transition-metal-catalyzed C-H functionalization at the remote C4/C7 positions, transition-metal-catalyzed cross-coupling, and transition-metal-free functionalization.

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