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 …

Water, as a green reaction medium, is safe, non-toxic, and rich in reserves on Earth, while
visible light represents a renewable, clean, and abundant energy source. Organic …

Chalcogenative sulfones (thiosulfonates and selenosulfonates), as reactants for organic
transformations, are widely used and interesting because of their potential to react with …

Radical remote 1, n-difunctionalization reactions (n> 2) of alkenes are powerful tools to
efficiently introduce functional groups with selected distances into target molecules. Among …

Advances in visible light-photocatalyzed preparative synthetic organic transformations in
water or aqueous media are studied. Both the convenience of visible light photocatalytic …

We report a metal-free trifluoromethylthiolation and trifluoromethylselenolation of 1, 4-
dihydropyridines with S-(trifluoromethyl) 4-methylbenzenesulfonothioate and Se …

Herein we report the development of deacylative thiolation of diverse methyl ketones. The
reaction is redox‐neutral, and heavy‐metal‐free, which provides a new way to introduce …

The application of water in chemical synthesis has been a hot research field in green and
sustainable chemistry. With the development of photochemical synthesis, photocatalysis in …

The radical 1, 5-chloropentafluorosulfanylation of vinyl cyclopropanes (VCPs) initiated by
Et3B/O2 affords allylic pentafluorosulfanyl/homoallylic chloride products through the ring …

With in-depth research on 1, 2-difunctionalization, remote difunctionalization has garnered
widespread attention for achieving multifunctionality. Herein, we report a strategy for …