A visible light-promoted hydrosilylation of alkynes has been explored and achieved using 1 mol % organic dye Eosin Y as the photocatalyst and a catalytic amount of thiol as the radical quencher. The corresponding alkenylsilanes were provided with high regio- and stereoselectivites in the reactions of various terminal and internal alkynes. The experimental evidence shows that the reaction is preferentially initiated by a single electron transfer process, and a photoredox pathway is suggested
A convenient visible-light photoredox catalysis has been developed for the synthesis of thioesters f...
Radical group transfer is a powerful tool for the formation of C–C bonds. These processes typically ...
Light-induced Brook rearrangements of acylsilanes facilitate silylacylation reactions of electron-de...
A visible light-driven radical hydrosilylation of electron-neutral and -rich alkenes has been invest...
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A...
In the last decades, photochemistry has been at the forefront of organic chemistry as a modern tool ...
Herein, we report light-promoted photo/hydrogen atom transfer dual catalysis for arylsilylation of a...
Manganese-photocatalyzed activation of the Si–H bond in silanes for the hydrosilylation of alkynes h...
An efficient iminyl radical-triggered 1,5-hydrogen-atom transfer/Heck-type coupling cascade has been...
The Direct oxidative cleavage of activated alkynes via hydroamination has been described using organ...
Ethynylbenziodoxolones (EBXs) have recently emerged as potent reagents for the alkynylation of radic...
Iridium complexes are known catalysts for a range of silylation reactions. However, the exploitation...
Sulfonyl chlorides are inexpensive reactants extensively explored for functionalization, but never c...
The photocatalytic reaction of o-methylthio-arenediazonium salts with alkynes yields substituted ben...
The eosin Y-catalyzed hydroperfluoroalkylation of electron-deficient alkenes is described herein. Th...
A convenient visible-light photoredox catalysis has been developed for the synthesis of thioesters f...
Radical group transfer is a powerful tool for the formation of C–C bonds. These processes typically ...
Light-induced Brook rearrangements of acylsilanes facilitate silylacylation reactions of electron-de...
A visible light-driven radical hydrosilylation of electron-neutral and -rich alkenes has been invest...
Herein, a one-step chlorosulfonylation of alkynes via a photocatalytic redox process is described. A...
In the last decades, photochemistry has been at the forefront of organic chemistry as a modern tool ...
Herein, we report light-promoted photo/hydrogen atom transfer dual catalysis for arylsilylation of a...
Manganese-photocatalyzed activation of the Si–H bond in silanes for the hydrosilylation of alkynes h...
An efficient iminyl radical-triggered 1,5-hydrogen-atom transfer/Heck-type coupling cascade has been...
The Direct oxidative cleavage of activated alkynes via hydroamination has been described using organ...
Ethynylbenziodoxolones (EBXs) have recently emerged as potent reagents for the alkynylation of radic...
Iridium complexes are known catalysts for a range of silylation reactions. However, the exploitation...
Sulfonyl chlorides are inexpensive reactants extensively explored for functionalization, but never c...
The photocatalytic reaction of o-methylthio-arenediazonium salts with alkynes yields substituted ben...
The eosin Y-catalyzed hydroperfluoroalkylation of electron-deficient alkenes is described herein. Th...
A convenient visible-light photoredox catalysis has been developed for the synthesis of thioesters f...
Radical group transfer is a powerful tool for the formation of C–C bonds. These processes typically ...
Light-induced Brook rearrangements of acylsilanes facilitate silylacylation reactions of electron-de...