Alkenes are valuable feedstocks in organic synthesis. Selenium or sulfur‐containing
coumpounds with a neighboring functional group can be easily prepared by direct …

Organoselenium chemistry has become a renewed topic in synthetic organic chemistry
mainly because of its successful application in biological, medicinal, and material sciences …

A calcium-mediated three-component selenylation of gem-difluoroalkenes using alcohols as
nucleophiles and N-(phenylseleno) phthalimide as the selenylation agent has been …

Three-component selenofunctionalization processes of olefins, diselenides and
sulfonamides, water, alcohols, or acids utilizing 1-fluoropyridinium triflate (FP-OTf) as a …

A visible‐light‐induced method was developed to synthesize selenylated cyclic boronic
esters through intermolecular oxyselenenylation. This method can be performed under …

The installation of selenium groups has become an essential step across a number of
industries such as agrochemicals, drug discovery, and materials. However, direct C (sp3)–H …

This work demonstrates the electrochemical construction of 2-methyl-1-aryloxy-3-
(arylselanyl) propan-2-ol/2-hydroxy-2-methyl-3-(arylselanyl) propyl 2-(2-hydroxy-2-methyl-3 …

A white light/iodosuccinimide (NIS)‐promoted three component reaction of alkenes, N‐
sulfonylhydrazones, and diorganyl diselenides for synthesis of organylselenylethyl …

Oxime esters are useful scaffolds in many organic chemistry transformations. Herein, a novel
visible-light-mediated three-component reaction for synthesis of oxime esters is reported …

We report a light-promoted hydroselenation of alkenes with high anti-Markovnikov
selectivity. Blue light activates an aryl diselenide to generate a seleno radical with …