{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Paul A"],"funding":["National Institute of General Medical Sciences","NIGMS NIH HHS"],"pagination":["1224-1227"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9039734"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["24(5)"],"pubmed_abstract":["Relatively unstable cyclic imines, generated in situ from their corresponding alicyclic amines via oxidation of their lithium amides with simple ketone oxidants, engage aryllithium compounds containing a leaving group on an <i>ortho</i>-methylene functionality to provide polycyclic isoindolines in a single operation. The scope of this transformation includes pyrrolidine, piperidine, azepane, azocane, and piperazines."],"journal":["Organic letters"],"pubmed_title":["Synthesis of Polycyclic Isoindolines via α-C-H/N-H Annulation of Alicyclic Amines."],"pmcid":["PMC9039734"],"funding_grant_id":["R01GM101389","R01 GM101389"],"pubmed_authors":["Vasseur C","Paul A","Daniel SD","Seidel D"],"additional_accession":[]},"is_claimable":false,"name":"Synthesis of Polycyclic Isoindolines via α-C-H/N-H Annulation of Alicyclic Amines.","description":"Relatively unstable cyclic imines, generated in situ from their corresponding alicyclic amines via oxidation of their lithium amides with simple ketone oxidants, engage aryllithium compounds containing a leaving group on an <i>ortho</i>-methylene functionality to provide polycyclic isoindolines in a single operation. The scope of this transformation includes pyrrolidine, piperidine, azepane, azocane, and piperazines.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Feb","modification":"2025-04-18T15:53:13.076Z","creation":"2025-04-07T02:48:12.635Z"},"accession":"S-EPMC9039734","cross_references":{"pubmed":["35100511"],"doi":["10.1021/acs.orglett.2c00018"]}}