Fig. 1: Strategies in C–H functionalization of (hetero)aromatic compounds. | Nature Communications

Fig. 1: Strategies in C–H functionalization of (hetero)aromatic compounds.

From: Catalyst-controlled directing group translocation in the site selective C–H functionalization of 3-carboxamide indoles and metallocarbenes

Fig. 1

a Transient directing groups in transition metal-catalyzed C–H activations. b Pre-installed directing groups in assorted metallocarbene C–H insertions. c The ester ‘dance’ reaction developed by Yamaguchi. d Selected natural products bearing the 2,3-disubstituted indole scaffold; e This work: a transition metal-catalyzed sequential  indole carboxamide translocation/C3-functionalization with metallocarbenes.

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