Organosulfur compounds have long played a vital role in organic chemistry and in the
development of novel chemical structures and architectures. Prominent among these …

1, 2, 3, 5-Tetrakis (carbazol-9-yl)-4, 6-dicyanobenzene (4CzIPN) is a typical donor–acceptor
fluorophore, with carbazolyl as an electron donor and dicyanobenzene as an electron …

The difunctionalizative trifluoromethylation of unsaturated C− C bonds is a highly useful and
efficient method for the synthesis of trifluoromethyl compounds with attractive architectures …

Electrosynthesis can be considered a powerful and sustainable methodology for the
synthesis of small organic molecules. Due to its intrinsic ability to generate highly reactive …

Herein, a radical–radical cross-coupling strategy for direct difluoromethylation of the C (sp3)–
H bond is reported. This transformation was readily accomplished under transition metal …

A visible-light-initiated trifluoromethylation/remote aliphatic C–H alkynylation of α-alkyl-
substituted vinyl azides using acetylenic triflones as both the trifluoromethyl and alkyne …

A step-economical method for synthesis of α-CF2H-substituted ketones from readily
available alkene feedstocks has been developed. Radical difluoromethylation of aromatic …

We describe the preparation of S‐perfluoroalkyl benzodithiazole trioxides as radical
perfluoroalkylating reagents. Their syntheses were performed on a multi‐gram scale by an …

Syntheses of chemicals using renewable electricity and when generating high atom
economies are considered green and sustainable processes. In the present state of affairs …

Electrochemical oxidative radical trifluoromethylation/semipinacol rearrangement
sequences of alkenyl alcohols were developed in this study. This approach is …