Driven by the continuous demand for sustainable organic synthesis, the field of
photocatalysis has emerged as a powerful manifold for direct modification of various …

The radical acylated difunctionalization of unsaturated carbon–carbon bonds, which
introduces acyl and other groups simultaneously, represents an attractive approach for the …

The use of visible light and photoredox catalysis emerged as a powerful and sustainable
tool for organic synthesis, showing high value for distinctly different ways of bond creation …

Here, we show the conversion of unactivated alkenes into α‐branched enones via
regioselective chloroacylation with acyl chlorides. The method relies upon the initial in situ …

We herein describe a simple approach for generating acyl radical from acyl chloride via
photoinduced single-electron transfer. It has been demonstrated that the generated acyl …

Acyl fluorides are versatile reagents in organic synthesis. However, there is no precedent to
employ acyl fluorides as acyl radical precursors. We herein report an N-heterocyclic …

Halogenation is one of the most important transformations in organic synthesis.
Halogenated compounds are employed in many reactions to prepare useful molecules …

Alkyloxalyl chlorides, generated from alcohols and oxalyl chlorides, are used as
alkoxycarbonyl radicals in the reaction of N-acryloyl benzamides under photocatalysis at …

A visible-light-induced three-component alkoxyalkylation of alkenes has been developed
under the photocatalysis of fac-Ir (ppy) 3. The alkene substrate scope included aryl and …

We herein report an efficient photoredox radical cyclization reaction of o-vinylaryl
isocyanides with acyl chlorides to access a wide range of 2, 4-disubstituted quinolines …