<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(23)</volume><submitter>Morlacci V</submitter><pubmed_abstract>An electrochemical initiated tandem reaction of anilines with 2-formyl benzonitrile has been developed. Thus, unprecedented 3-N-aryl substituted isoindolinones have been conveniently achieved by constant current electrolysis in a divided cell using catalytic amount of electricity and supporting electrolyte and a Pt-cathode as working electrode. The origin of the electrochemical activation as well as the mechanism of the subsequent chemical cascade reactions have been investigated by DFT calculations.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>8199</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9738245</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Electrochemical-Induced Cascade Reaction of 2-Formyl Benzonitrile with Anilines: Synthesis of N-Aryl Isoindolinones.</pubmed_title><pmcid>PMC9738245</pmcid><pubmed_authors>Palombi L</pubmed_authors><pubmed_authors>Aschi M</pubmed_authors><pubmed_authors>Morlacci V</pubmed_authors><pubmed_authors>Caruso T</pubmed_authors><pubmed_authors>Chiarini M</pubmed_authors><pubmed_authors>Arcadi A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical-Induced Cascade Reaction of 2-Formyl Benzonitrile with Anilines: Synthesis of N-Aryl Isoindolinones.</name><description>An electrochemical initiated tandem reaction of anilines with 2-formyl benzonitrile has been developed. Thus, unprecedented 3-N-aryl substituted isoindolinones have been conveniently achieved by constant current electrolysis in a divided cell using catalytic amount of electricity and supporting electrolyte and a Pt-cathode as working electrode. The origin of the electrochemical activation as well as the mechanism of the subsequent chemical cascade reactions have been investigated by DFT calculations.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-20T03:30:43.974Z</modification><creation>2025-04-20T03:30:43.974Z</creation></dates><accession>S-EPMC9738245</accession><cross_references><pubmed>36500288</pubmed><doi>10.3390/molecules27238199</doi></cross_references></HashMap>