We are entering an era that emphasizes greenness and sustainability. Based on such a
philosophy, it is critical to uncover novel and original sustainable reaction modes for future …

Transition metal-catalyzed direct functionalization of C–H bonds is one of the key emerging
strategies that is currently attracting tremendous attention with the aim to provide alternative …

Over the last decade, substantial research has led to the introduction of an impressive
number of efficient procedures which allow the selective construction of C C bonds by …

The direct C3-functionalization of quinoxalin-2 (1H)-ones via C–H bond activation has
recently attracted considerable attention, due to their diverse biological activities and …

An efficient and concise one-pot protocol to synthesize sulfonylated quinoline N-oxides via
copper-catalyzed C–H bond activation has been developed. Commercially available and …

The catalytic cross‐dehydrogenative coupling (CDC) reaction has received intense attention
in recent years. The attractive feature of this coupling process is the formation of a C C …

Oxidative coupling between C (sp2)–H bonds and C (sp3)–H bonds is achieved by the Ni (II)-
catalyzed reaction of benzamides containing an 8-aminoquinoline moiety as the directing …

A convenient and efficient transition-metal-free protocol for the synthesis of 3-alkyl
quinoxalin-2 (1H)-ones from the radical reaction of quinoxalin-2 (1H)-ones with ethers was …

A Cu-catalyzed method has been identified for selective oxidative arylation of benzylic C–H
bonds with arylboronic esters. The resulting 1, 1-diarylalkanes are accessed directly from …

The development of practical and efficient methods for C–C and C–X bond formation has
attracted a great deal of current attention with the advent of C–H functionalization reactions …