<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>61(49)</volume><submitter>Zhao F</submitter><funding>China Scholarship Council</funding><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.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>e202214812</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10100518</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Copper-Catalyzed 1,2-Dicarbonylative Cyclization of Alkenes with Alkyl Bromides via Radical Cascade Process.</pubmed_title><pmcid>PMC10100518</pmcid><pubmed_authors>Zhao F</pubmed_authors><pubmed_authors>Franke R</pubmed_authors><pubmed_authors>Gu XW</pubmed_authors><pubmed_authors>Wu XF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Copper-Catalyzed 1,2-Dicarbonylative Cyclization of Alkenes with Alkyl Bromides via Radical Cascade Process.</name><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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-18T21:20:17.375Z</modification><creation>2025-02-18T23:40:31.815Z</creation></dates><accession>S-EPMC10100518</accession><cross_references><pubmed>36254794</pubmed><doi>10.1002/anie.202214812</doi></cross_references></HashMap>