{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["61(49)"],"submitter":["Zhao F"],"funding":["China Scholarship Council"],"pubmed_abstract":["Herein, we developed a new procedure on 1,2-dicarbonylative cyclization of 4-aryl-1-butenes with alkyl bromides. Using simple copper catalyst, two molecules of carbon monoxide were introduced into the double bond with the formation of four new C-C bonds and a new ring. Various α-tetralones and 2,3-dihydroquinolin-4-ones were formed in moderate to good yields."],"journal":["Angewandte Chemie (International ed. in English)"],"pagination":["e202214812"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10100518"],"repository":["biostudies-literature"],"pubmed_title":["Copper-Catalyzed 1,2-Dicarbonylative Cyclization of Alkenes with Alkyl Bromides via Radical Cascade Process."],"pmcid":["PMC10100518"],"pubmed_authors":["Zhao F","Franke R","Gu XW","Wu XF"],"additional_accession":[]},"is_claimable":false,"name":"Copper-Catalyzed 1,2-Dicarbonylative Cyclization of Alkenes with Alkyl Bromides via Radical Cascade Process.","description":"Herein, we developed a new procedure on 1,2-dicarbonylative cyclization of 4-aryl-1-butenes with alkyl bromides. Using simple copper catalyst, two molecules of carbon monoxide were introduced into the double bond with the formation of four new C-C bonds and a new ring. Various α-tetralones and 2,3-dihydroquinolin-4-ones were formed in moderate to good yields.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Dec","modification":"2025-04-18T21:20:17.375Z","creation":"2025-02-18T23:40:31.815Z"},"accession":"S-EPMC10100518","cross_references":{"pubmed":["36254794"],"doi":["10.1002/anie.202214812"]}}