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 …

Spirocyclobutyl oxindoles have garnered substantial attention in drug discovery and
pharmaceuticals owing to their wide range of biological activities. Strain-release in small …

β-Amino sulfones find extensive applications in pharmaceuticals, natural products,
agrochemicals, and organic synthesis. Meanwhile, aziridine units are recognized as …

A photoinduced EnT-mediated generation of sulfonamidyl radicals has been accomplished
using rationally designed iminophenylacetic acid oxime ester reagents under metal-free …

Sulfur (VI)‐based functional groups are popular scaffolds in a wide variety of research fields
including synthetic and medicinal chemistry, as well as chemical biology. The growing …

Sulfonamides are important structures in pharmaceuticals, agrochemicals, and
organocatalysts, yet the rapid and benign synthesis of these compounds is still a great …

Over the past decade, visible-light-mediated energy-transfer (EnT) catalysis, particularly
triplet–triplet energy-transfer (TTEnT) catalysis, has emerged as a mild and environmentally …

A metal-free photosensitized 1, 2-imino-sulfamoylation of olefins by employing a tailor-made
sulfamoyl carbamate as the difunctionalization reagent has been established. This protocol …

Nitrogen central radicals (NCRs) are versatile synthetic intermediates for creating functional
nitrogen-containing molecules. Herein, a photosensitized β-sulfonylamination of terminal …

IIn this paper, a visible‐light‐induced intramolecular [2+ 2] cycloaddition has been revealed
to synthesize the bishomocubanone derivatives in moderate to excellent yield under mild …