Difunctionalization of alkenes enables construction of complex compounds in one pot. In this
report, we presented an intermolecular, redox‐neutral three‐component …

Visible‐light photoredox catalysis has been utilized in a new multicomponent reaction
forming β‐functionalized δ‐diketones under mild conditions in an operationally convenient …

Abstract We report the 1, 6-addition of acyl radicals to the electron-deficient 1, 3-dienes
under visible-light photoredox catalysis. The deoxygenative allylation of the carboxylic acid …

A mild and inexpensive approach to synthesising a series of 1, 4-diketones in moderate to
excellent yields via 1, 2-oxo alkylation has been developed using fluorescein as a …

A photoredox-catalyzed divergent 1, 2-dicarbonylation and hydroacylation of alkenes with
acid anhydride is presented. This approach offers a mild and efficient entry to 1, 4-dicarbonyl …

Alkenes and their related analogs are ideal starting materials for organic synthesis, and the
selective difunctionalization of alkenes, which allows the simultaneous introduction of two …

A photoredox-catalyzed alkylarylation of activated alkenes via a radical C–C bond
cleavage/Truce–Smiles rearrangement cascade is developed. The protocol features mild …

We report the development of a photocatalytic strategy for the synthesis of β-functionalized
unsymmetrical 1, 4-, 1, 6-, and 1, 7-diketones from aroyl chlorides and unactivated alkenes …

Comprehensive Summary The radical‐mediated reductive functionalization of aryl halides
has been extensively studied. However, the related radical‐mediated intermolecular …

A novel photoredox catalysis for multiple functionalization of two different types of
unactivated alkenes in a single operation was reported through a conceptually new mode of …