In recent years, palladium-catalysed arylation of heteroaromatics via C–H bond activation
has become a popular method for generating carbon–carbon bonds. For this reaction, a …

In the past decade, direct arylation polymerization (DArP) has rapidly developed as a
sustainable synthetic protocol for cost‐effective, atom‐economical preparation of conjugated …

A long‐standing challenge in Minisci reactions is achieving the arylation of heteroarenes by
oxidative decarboxylation of aromatic carboxylic acids. To address this challenge, the silver …

CH activation involves any of a wide range of techniques, often using catalysts in which a
carbon to hydrogen covalent bond of an organic compound is cleaved to replace the …

A sequential procedure for the synthesis of 2, 5-disubstituted thiazoles from terminal
alkynes, sulfonyl azides, and thionoesters is reported. A copper (I)-catalyzed 1, 3-dipolar …

Asymmetric C− H bond functionalization reaction is one of the most efficient and
straightforward methods for the synthesis of optically active molecules. Herein we disclose …

Passive membrane permeability is a fundamental challenge in the development of bioactive
macrocycles. To achieve this objective, chemists have resorted to various strategies, the …

On the basis of the strategy of developing highly efficient protocol for Pd-catalyzed cross-
coupling reactions, a series of bulky bis (imino) acenaphthene (BIAN)-supported Pd-PEPPSI …

A general approach to the synthesis of diverse heteroaryl-C-Δ1, 2-glycosides has been
developed by employing the Pd (OAc) 2/CuI cocatalyzed direct cross-coupling of five …

An efficient method has been developed to afford highly C-5 selective olefination of thiazole
derivatives utilizing a bifunctional template in an intermolecular fashion. Coordinative …