Dearomatization of indole derivatives offers a straightforward approach to access diverse
indolines. To date, the corresponding dearomative transformations involving electron …

Indole dearomatization has been achieved via radical hydroarylation. Under mild
photoredox conditions, a range of indole derivatives undergo hydroarylation to form 2 …

A photocatalytic protocol for the divergent dearomative functionalization of indole derivatives
is reported. Under the irradiation of visible light, either dimerization or reduction occurs …

The dearomatization of indoles represents the most efficient approach for accessing highly
valued indolines. The inherent nucleophilic reactivity of indoles has dictated indole …

Dearomatization of indoles provides efficient synthetic routes for substituted indolines. In
most cases, indoles serve as nucleophiles. Reported here is an asymmetric dearomatization …

Accessing fascinating organic and biological significant indolines via dearomatization of
indoles represents one of the most efficient approaches. However, it has been difficult for the …

Described is an efficient oxidative dearomatization of indoles with TEMPO oxoammonium
salt and a broad range of nucleophiles. Under very mild conditions, dearomative …

An efficient synthesis of methylene-unsubstituted cyclopropane-fused indolines via
photoredox catalyzed dearomative cyclopropanation of indole derivatives was developed. A …

We report herein a convenient and scalable dearomative hydroacylation reaction of indoles.
Employing readily available aldehydes as the acyl source and TBADT as an inexpensive …

Prenylated and reverse-prenylated indolines are privileged scaffolds in numerous naturally
occurring indole alkaloids with a broad spectrum of important biological properties …