Herein, we report a three-component organophotoredox coupling of N-alkenyl amides with α-
bromocarbonyls and various nucleophiles. This transition metal-free difunctionalization …

The ability to selectively synthesize multiple products from the same sets of substrates is a
highly appealing and challenging concept in synthetic chemistry. In this manuscript, we …

Visible light induced photoredox catalysis is an efficient method for radical activation.
Herein, we report the photoredox catalysis involving an intramolecular radical–radical …

A strategy with arylidene malonates provides access to β-umpolung single-electron species.
Reported here is the utilization of these operators in intermolecular radical–radical …

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 …

Herein, we describe a method for the direct decarboxylative C–N coupling of carboxylic
acids with a range of nitrogen nucleophiles. This platform employs visible-light-mediated …

Visible-light-mediated tandem radical difluoroalkylation and alkynylation of unactivated
alkenes is described in this communication. The process comprises a mild C–C bond …

The radical difunctionalization of alkenes with sulfonyl bifunctional represents a powerful
and straightforward approach to access functionalized alkane derivatives. However, both the …

A radical relay strategy is described to synthesize functionalized β-amino alcohols. This
strategy is enabled by photoredox-catalyzed and nitrogen-centered radical-triggered …

The In (OTf) 3-promoted three-component photoredox alkylarylation of styrenes with alkyl
NHP esters and arenes to access alkylated arene derivatives through C–C bond cleavage …