Polycyclic indole scaffolds are ubiquitous in pharmaceuticals and natural products and in
materials science. Here, we present a visible-light-initiated intramolecular aryl migration …

Based on the importance of the two classes of nitrogen-containing heterocyclic structures,
isoindolinones and isoquinolinones, herein, through intramolecular cascade cyclization via …

In the present studies, we describe a convenient and efficient protocol for the synthesis of
the indolo [2, 1-α] isoquinoline core structure through the reaction of 2-aryl-N-acryloyl …

We describe a photocatalyzed transformation for the synthesis of the indolo [2, 1-a]
isoquinoline core structure. This redox neutral reaction features mild reaction conditions and …

Nitrogen heterocycles, especially polycyclic compounds, are significant skeletons in
valuable molecules. Herein, we developed an efficient and practical visible-light-induced …

We have developed a metal-free radical cascade reaction of N-substituted 2-aryl indoles
with readily available sulfonyl hydrazides for the rapid construction of arylsulfonyl …

Pyrrolo [1, 2-a] indoles are structurally important scaffolds in many natural products and
bioactive compounds. Herein, we report a novel synthetic method for pyrrolo [1, 2-a] indole …

An efficient N-centered radical intramolecular cyclization reaction of alkenyl amides induced
by visible light was described. In this process, an alkenyl amide underwent 5-exo/6-endo …

A transition metal-free photoredox cascade cyclization is herein reported. In this protocol,
sustainable visible light was used as the energy source and organic light-emitting molecule …

We report a convenient process for synthesizing indolo-[2, 1-a] isoquinoline tetracyclic
skeletons in one pot via a low-cost copper-catalyzed tandem amino radical cyclization, in …