Electrochemistry has recently gained increased attention as a versatile strategy for
achieving challenging transformations at the forefront of synthetic organic chemistry …

Three‐membered carbocyclic and heterocyclic ring structures are versatile synthetic
building blocks in organic synthesis with biological importance. Moreover, the inherent strain …

In this work, novel cross-linked chitosan by the G1 dendrimer from condensation of
melamine and toluene-2, 4-diisocyante terminated by sulfamic acid groups (CS-TDI-Me-TDI …

A unique, facile, and straightforward electrochemical oxidative annulation of inactivated
propargyl aryl ethers with sulfonyl hydrazides leading to 3-sulfonated 2 H-chromenes has …

Electronically unbiased arylcyclopropane functionalization has always been a challenge to
organic chemists, and the emergence of donor–acceptor cyclopropanes (DACs) has not …

An efficient iodine-mediated electrochemical C (sp3)–H cyclization was developed under
mild conditions. A variety of functionalized quinazolinone-fused N-heterocycles can be …

An unprecedented external oxidant‐free electrochemical protocol for 1, 3‐oxohydroxylation
of donor‐acceptor cyclopropane is disclosed. The strategy encompasses the activation of …

Nonsymmetrical malonamides are often found in pharmacologically relevant molecules. A
flexible and atom-economical method is developed for efficient preparation of …

Azomethine ylides are fascinating 1, 3-dipoles for [3+ 2] cycloaddition reactions toward the
construction of N-heterocycles. Herein, an efficient and environmentally benign …

We have established a supporting‐electrolyte free electrochemical method for the synthesis
of indazolylindazolones through oxygen reduction reaction (eORR) induced 1, 3‐oxo …