<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(49)</volume><submitter>Bacaicoa S</submitter><funding>Adlerbertska Research Foundation</funding><funding>Stiftelserna Wilhelm och Martina Lundgrens</funding><pubmed_abstract>Herein, we present an accessible aerobic N-heterocyclic carbene (NHC)-catalyzed method that efficiently produces tetrasubstituted benzene rings in a single reaction. The method employs atmospheric oxygen (O&lt;sub>2&lt;/sub>) as the terminal oxidant in a reaction that requires two oxidative steps. The aerobic oxidation is achieved by a selection of electron transfer mediators orchestrating a redox cascade, turning a high-energy aerobic oxidation reaction pathway into a favorable process.</pubmed_abstract><journal>Organic letters</journal><pagination>9146-9150</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9764416</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aerobic Oxidative N-Heterocyclic Carbene-Catalyzed Formal [3+3] Cyclization for the Synthesis of Tetrasubstituted Benzene Derivatives.</pubmed_title><pmcid>PMC9764416</pmcid><pubmed_authors>Goossens E</pubmed_authors><pubmed_authors>Sunden H</pubmed_authors><pubmed_authors>Bacaicoa S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aerobic Oxidative N-Heterocyclic Carbene-Catalyzed Formal [3+3] Cyclization for the Synthesis of Tetrasubstituted Benzene Derivatives.</name><description>Herein, we present an accessible aerobic N-heterocyclic carbene (NHC)-catalyzed method that efficiently produces tetrasubstituted benzene rings in a single reaction. The method employs atmospheric oxygen (O&lt;sub>2&lt;/sub>) as the terminal oxidant in a reaction that requires two oxidative steps. The aerobic oxidation is achieved by a selection of electron transfer mediators orchestrating a redox cascade, turning a high-energy aerobic oxidation reaction pathway into a favorable process.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-26T09:43:06.701Z</modification><creation>2025-04-06T13:08:29.644Z</creation></dates><accession>S-EPMC9764416</accession><cross_references><pubmed>36469618</pubmed><doi>10.1021/acs.orglett.2c03879</doi></cross_references></HashMap>