| Literature DB >> 32975859 |
Anirudra Paul1, Jae Hyun Kim1,2, Scott D Daniel1, Daniel Seidel1.
Abstract
Despite extensive efforts by many practitioners in the field, methods for the direct α-C-H bond functionalization of unprotected alicyclic amines remain rare. A new advance in this area utilizes N-lithiated alicyclic amines. These readily accessible intermediates are converted to transient imines through the action of a simple ketone oxidant, followed by alkylation with a β-ketoacid under mild conditions to provide valuable β-amino ketones with unprecedented ease. Regioselective α'-alkylation is achieved for substrates with existing α-substituents. The method is further applicable to the convenient one-pot synthesis of polycyclic dihydroquinolones through the incorporation of a SN Ar step.Entities:
Keywords: C−C bond formation; C−H bond functionalization; Mannich reaction; alicyclic amines; annulation
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Year: 2020 PMID: 32975859 PMCID: PMC7854982 DOI: 10.1002/anie.202011641
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336