{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["20"],"submitter":["Mari G"],"pubmed_abstract":["A new class of heterocyclic <i>N</i>,<i>O</i>-aminal and hemiaminal scaffolds was successfully obtained by means of a three-component reaction (3-CR) of 1,2-diaza-1,3-dienes (DDs), α-aminoacetals and iso(thio)cyanates. These stable imine surrogates are generated from key-substituted (thio)hydantoin intermediates through selective FeCl<sub>3</sub>-catalyzed intramolecular <i>N</i>-annulation."],"journal":["Beilstein journal of organic chemistry"],"pagination":["1412-1420"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11216082"],"repository":["biostudies-literature"],"pubmed_title":["Challenge <i>N</i>- versus <i>O</i>-six-membered annulation: FeCl<sub>3</sub>-catalyzed synthesis of heterocyclic <i>N</i>,<i>O</i>-aminals."],"pmcid":["PMC11216082"],"pubmed_authors":["Mari G","Favi G","Olivieri D","Santeusanio S","Mantellini F","De Crescentini L"],"additional_accession":[]},"is_claimable":false,"name":"Challenge <i>N</i>- versus <i>O</i>-six-membered annulation: FeCl<sub>3</sub>-catalyzed synthesis of heterocyclic <i>N</i>,<i>O</i>-aminals.","description":"A new class of heterocyclic <i>N</i>,<i>O</i>-aminal and hemiaminal scaffolds was successfully obtained by means of a three-component reaction (3-CR) of 1,2-diaza-1,3-dienes (DDs), α-aminoacetals and iso(thio)cyanates. These stable imine surrogates are generated from key-substituted (thio)hydantoin intermediates through selective FeCl<sub>3</sub>-catalyzed intramolecular <i>N</i>-annulation.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024","modification":"2025-04-22T12:02:12.435Z","creation":"2025-04-06T00:13:49.875Z"},"accession":"S-EPMC11216082","cross_references":{"pubmed":["38952961"],"doi":["10.3762/bjoc.20.123"]}}