A unified strategy involving visible‐light‐induced iminyl‐radical formation has been
established for the construction of pyridines, quinolines, and phenanthridines from acyl …

The visible‐light‐promoted decarboxylation of α‐imino‐oxy propionic acids for the
generation of iminyl radicals has been accomplished through the use of Ir (dFCF3ppy) 2 …

A photoredox‐catalyzed iminoalkenylation of γ‐alkenyl O‐acyl oximes has been developed.
Readily available alkenylboronic acids serve as alkenylation reagents, leading to densely …

An efficient strategy assisted by visible-light-promoted iminyl radical formation has been
developed for the synthesis of 6-(fluoro) alkylated phenanthridine derivatives. In the …

The intramolecular 1, 5-H transfer reaction of the aryl radicals generated from unactivated
aryl iodides by photocatalysis is described. The features of this transformation are …

A visible‐light‐driven radical‐mediated strategy for the in situ generation of aza‐ortho‐
quinone methides from 2‐vinyl‐substituted anilines and alkyl radical precursors is …

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 …

A one-pot synthesis of phenanthridines and quinolines from commercially available or easily
prepared aldehydes has been reported. O-(4-Cyanobenzoyl) hydroxylamine was utilized as …

N‐Acyliminoiodinanes were characterized for the first time by X‐ray structural analysis. The
ortho‐methoxymethyl group and the carbonyl oxygen coordinate to the iodine atom of the …

A straightforward synthetic strategy to construct biologically relevant phenanthridinones and
quinolinones was developed via visible-light-promoted direct oxidative C–H amidation. In …