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This protocol constitutes an efficient route to difluoroamidated indenylquinolines, wherein the difluorobromoamide functions as the electron acceptor and (NH4)2S2O8 serves as the electron donor. The method is distinguished by mild reaction conditions, operational simplicity, metal-free catalysis, excellent functional group tolerance, and a broad substrate scope.<\/jats:p>","DOI":"10.1021\/acs.joc.6c01033","type":"journal-article","created":{"date-parts":[[2026,7,16]],"date-time":"2026-07-16T13:32:30Z","timestamp":1784208750000},"page":"10490-10496","source":"Crossref","is-referenced-by-count":0,"title":["Visible-Light-Induced\nRadical Cascade Cyclization\nof 1,7-Enynes to Access CF2-Containing Indenoquinolines\nby an Electron Donor"],"prefix":"10.1021","volume":"91","author":[{"given":"Zhen","family":"Chen","sequence":"first","affiliation":[{"name":"Yangzhou University , , ,","place":["Yangzhou, P. R. 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