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This newly developed reductive aminocarbonylation reaction operates efficiently at ambient temperature (25 \u00b0C) in the absence of an external photocatalyst. Both aryl and alkenyl iodides were suitable substrates, providing access to a wide range of substituted amides in good to excellent yields. The exceptionally mild reaction conditions significantly improve functional group compatibility, thereby expanding the substrate scope of this transformation.<\/jats:p>","DOI":"10.1021\/acs.joc.6c01457","type":"journal-article","created":{"date-parts":[[2026,8,19]],"date-time":"2026-08-19T04:02:08Z","timestamp":1787112128000},"page":"11831-11839","source":"Crossref","is-referenced-by-count":0,"title":["Visible-Light-Promoted\nPalladium-Catalyzed Aminocarbonylation\nof Aryl\/Alkenyl Iodides with Nitroarenes and Mo(CO)6"],"prefix":"10.1021","volume":"91","author":[{"given":"Jia-Ying","family":"Li","sequence":"first","affiliation":[{"name":"Wuyi University , , , ,","place":["Jiangmen, Guangdong, P. R. China, 529020"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wen-Hua","family":"Gao","sequence":"additional","affiliation":[{"name":"Wuyi University , , , ,","place":["Jiangmen, Guangdong, P. R. 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