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About the Cover:A radical reductive dearomatization of indoles is re-ported by Yang, Li, Bai, Zhang and Shi on page 1699. Under photoredox catalysis, the reaction employs N,N-diiso- propylethylamine (DIPEA) as an organic reductant and proceeds under mild conditions. Both 2-substituted and 2-unsubstituted indoles are well tol-erated, affording a series of structurally diverse func-tionalized indoline derivatives. -
About the Cover:Four types of radical-mediated 1,2,n-trifunctionalization strategies of olefins, namely radical addition/migration/ functionalization, cycload-dition/ring-opening/migration/ functionalization, al-lylic/alkenyl sequential functionalization, and multi-functional reagent-promoted polyfunctionalization, are reviewed by Lu, Qi, Zhang, Jin, Cao and Zhang on page 1540. This review analyzes the challenges of these reactions and outlines future development directions, providing a systematic reference for the efficient syn-thesis of complex molecules and the development of green organic chemistry. -
About the Cover:Visible-light-catalyzed hydroamination, hydroami-dation, and hydrosulfonamidation of alkenes are re-viewed by Zhang, Jia, Yu, Wu, Li, and Shu on page 1166. This review summarizes recent advances in the direct coupling of readily available alkenes with various nitrogen sources under mild visible-light irradiation. Particular emphasis is focused on representative cata-lytic modes involving single-electron transfer, pro-ton-coupled electron transfer, and hydrogen atom transfer pathways, as well as their selectivity control and substrate scope. -
About the Cover:Photoredox-catalyzed dicarbofunctionalization of alky- nes has become a cutting-edge research area in organic synthesis. The latest advances in this field are reviewed by Ye, and Yuan on page 1146, with an em-phasis on substrate scope, reaction mechanisms, selec-tivity control strategies, and synthetic applications, along with a forward-looking perspective on future developments.
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