The functionalisation of C–H bonds has been an enormous achievement in synthetic
methodology, enabling new retrosynthetic disconnections and affording simple synthetic …

Pyridine and its reduced form (piperidine) are the most common nitrogen heterocycles in
FDA-approved drugs. Additionally, their presence in alkaloids, ligands for transition metals …

para-Selective C–H functionalization of pyridines holds a significant value but remains
underdeveloped. Site-switchable C–H functionalization of pyridines under easily tunable …

Due to their strong covalent bonds and low reduction potentials, activating inert substrates is
challenging. Recent advances in photoredox catalysis offered a number of solutions, each of …

This work represents an important step in the quest for creating atomically precise binary
semiconductor nanoclusters (BS-NCs). Compared with coinage metal NCs, the preparation …

Catalytic carboxylation of C–H bonds using CO2 is a sustainable and economic strategy to
produce valuable carboxylic acids. However, this process presents challenges due to the …

Photoelectrochemistry is becoming an innovative approach to organic synthesis. Generally,
the current photoelectrocatalytic organic transformations suffer from limited reaction type …

Selective hydroarylation of dienes has potential to provide swift access to useful building
blocks. However, most existing methods rely on dienes stabilised by an aromatic group and …

C–H Functionalization of pyridines is an efficient strategy to access pyridine derivatives
occurring in pharmaceuticals, agrochemicals, and materials. Nucleophilic additions to …

p-Diarylboryl halothiophenols are developed and unequivocally characterized. Their
photophysical properties and catalytic performance are unveiled by experimental and …