Alkenes and their derivatives are featured widely in a variety of natural products,
pharmaceuticals, and advanced materials. Significant efforts have been made toward the …

We present here a review of the photochemical and electrochemical applications of multi-
site proton-coupled electron transfer (MS-PCET) in organic synthesis. MS-PCETs are redox …

Conspectus Oxidative cross-coupling has proved to be one of the most straightforward
strategies for forming carbon–carbon and carbon–heteroatom bonds from easily available …

The three-component reactions of enaminones, disulfides, and alcohols for the synthesis of
polyfunctionalized alkenes have been realized via the C–H and C–N bond transformation …

An efficient electrochemical approach for the C (sp2)–H phosphonation of quinoxalin-2 (1H)-
ones and C (sp3)–H phosphonation of xanthenes has been developed. The chemistry was …

We have developed a protocol for electrochemical decarboxylative C3 alkylation of a wide
range of quinoxalin-2 (1H)-ones under metal-and additive-free conditions. N …

Direct allylic C− H thiolation is straightforward for allylic C (sp3)− S bond formation.
However, strong interactions between thiol and transition metal catalysts lead to deactivation …

Heterocycles containing N and O are important structures in pharmaceuticals,
agrochemicals and functional molecules. The synthesis of these compounds usually …

By employing enaminones and thiuram disulfides as starting materials, the frontiers of
Newman–Kwart rearrangement have been expanded to the alkenyl system for the first time …

Enaminones are gaining increasing interest because of their unique properties and their
importance in organic synthesis as versatile building blocks. N, N-Dimethyl enaminones …