In the era of organic synthesis, the direct difunctionalization strategies of alkenes and
alkynes are very eminent, which open up an excellent route to introduce two functional …

The difunctionalizative trifluoromethylation of unsaturated C− C bonds is a highly useful and
efficient method for the synthesis of trifluoromethyl compounds with attractive architectures …

Precise stereocontrol of functionalized alkenes represents a long-standing research topic in
organic synthesis. Nevertheless, the development of a catalytic, easily tunable synthetic …

Popular and readily available alkenes and alkynes are good substrates for the preparation
of functionalized molecules through radical and/or ionic addition reactions …

An efficient intermolecular atom-transfer addition reaction of alkynes via the combination of
visible-light photoredox catalysis and gold catalysis has been developed, affording diverse …

In this study, we outline a general method for photocatalyzed difunctionalization of alkenes,
a diene, alkynes, 1, 3‐enynes, and [1.1. 1] propellane using dithiosulfonate reagents (ArSO2 …

Perfluoroalkylation is one of the most important methods for the introduction of multiple
fluorine atoms into organic molecules in a single step. The use of photoinduced technology …

We report the phosphine-catalyzed intermolecular carbofluorination of alkynes using acyl
fluorides as fluorinating reagents. This reaction promises to be a useful method for the …

A mild and efficient visible-light-induced atom transfer radical addition and cyclization of 1, n-
enynes (n= 6, 7) with perfluoroalkyl halides, leading to halo-perfluorinated N-heterocycles …

Photoredox catalysis has emerged as a strong synthetic tool for radical reactions. In
particular, a variety of regioselective difunctionalizations of carbon–carbon multiple bonds …