C–H/N–H cross-coupling has become a key technology for the selective conjugation of
azole drug molecules. However, the development of new synthetic models and green …

The ruthenium (II)-catalyzed tandem C–H allylation and intramolecular dipolar cycloaddition
between azomethine imines and 2-methylidenetrimethylene carbonate is described herein …

Reactive processing provides a simple approach for grafting dynamic covalent cross-linkers
onto linear or branched polymers, resulting in covalent adaptable networks (CANs). We …

We describe a simple, metal-free regioselective N2-arylation strategy for 5-substituted-1 H-
tetrazoles with diaryliodonium salts to access 2-aryl-5-substituted-tetrazoles. Diaryliodonium …

The structural modification of N-aryl indazolols as tautomers of N-aryl indazolones has been
established as a hot topic in pharmaceutics and medicinal chemistry. We herein disclose the …

A practical and scalable protocol for the regioselective C–H phenoxylation and azolation of
phenol derivatives via consecutive electro-oxidative CDC reaction has been demonstrated …

The structural modification of phthalazinones and indazolones has emerged as a pivotal
topic in catalytic C–H functionalization events. Herein we report the hydrazide-assisted …

Selective functionalization of a specific C (sp3)–H bond remains an open challenge in
synthetic chemistry. One common strategy employed by chemists to address this challenge …

Enzyme-catalyzed dynamic kinetic resolution was applied to the one-pot regio-and
enantioselective synthesis of 2, 5-disubstituted tetrazole hemiaminal esters, among which …

Reactive open-shell ring systems comprising C, N, O, and S atoms are crucial for the
radiation-induced molecular evolution and relevant to life and interstellar regions. Herein …