A photoinduced direct synthesis of 3‐amino‐1‐indenones via radical cascade cyclization
strategy is demonstrated. The methodology involves a domino reaction between 2 …

A direct and efficient visible-light-induced cascade cyclization reaction of aryl ynones with 4-
alkyl-DHPs for the divergent synthesis of indenones, thioflavones and spiro [5.5] trienones …

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 de novo method for direct construction of cyclopenta [b] indolines via a photocatalytic
fluoroalkylative radical cyclization cascade of ynamides has been established, which …

A visible light photoredox-catalyzed N-centered radical addition/semipinacol rearrangement
cascade of cycloalkanol-substituted 1H-indenes or styrenes with N-arylsulfonyl protected 1 …

Indenones are important scaffolds in natural products, biologically active molecules as well
as functional materials. Recently, radical cascade cyclization has emerged as an efficient …

Indoles are heterocyclic motifs that are embedded in a large number of bioactive natural
products and pharmaceuticals.[1] As such, the search for sustainable and more efficient …

We report a controlled radical cyclization cascade of isoquinoline-1, 3, 4 (2 H)-triones, 3-
hydroxyisoindolin-1-ones, and phthalimides from o-alkynylated benzamides by metal-free …

Low‐energy light, endowing with excellent characteristics of lower energy, fewer side
reactions, more abundance in solar light. The scenario has been developed for the …

Under photocatalytic reductive conditions, trifluoromethyl radical addition onto an ynamide
followed by cyclization on a benzoyl moiety produces diverse isoindolinone platforms with …