Conspectus The radical-mediated C–H functionalization of pyridines has attracted
considerable attention as a powerful tool in synthetic chemistry for the direct …

The use of organic photocatalysts has revolutionized the field of photoredox catalysis, as it
allows access to reactivities that were traditionally restricted to transition‐metal …

Ring structures such as pyridine, cyclopentane or their combinations are important motifs in
bioactive molecules. In contrast to previous cycloaddition reactions that necessitated a …

Covalent organic frameworks (COFs) are an outstanding platform for heterogeneous
photocatalysis. Herein, we synthesized a pyrene-based two-dimensional CC linked π …

Site-selective C–H functionalization in chemical feedstocks is a challenging and useful
reaction in the broad field of chemical research. Here, we report a modular photochemical …

A unified strategy for the deoxygenative or desulfurative pyridylation of various alcohols and
thiols has been developed through a single‐electron transfer (SET) process of frustrated …

By exploiting electron donor–acceptor (EDA) complexes between 1, 4-dihydropyridines and
N-amidopyridinium salts under visible light irradiation, we discovered that photoinduced …

The photoinduced C4-selective C–H borylation of pyridines was achieved using electron
donor–acceptor complexes derived from a Lewis base and N-amidopyridinium salts under …

Electron donor–acceptor (EDA) complex-mediated single-electron transfer (SET) is a crucial
method for generating carbon radicals. Hydrogen atom transfer (HAT) enables the direct …

Considering the synthetic relevance of heteroarenes in various areas ranging from organic
synthesis to medicinal chemistry, develo** practically simple methodologies to access …