| Literature DB >> 26371961 |
Kevin J Frankowski1,2, Ruzhang Liu1, Gregory L Milligan3, Kevin D Moeller4, Jeffrey Aubé5,6.
Abstract
Electrochemistry provides a powerful tool for the late-stage functionalization of complex lactams. A two-stage protocol for converting lactams, many of which can be prepared through the intramolecular Schmidt reaction of keto azides, is presented. In the first step, anodic oxidation in MeOH using a repurposed power source provides a convenient route to lactams bearing a methoxy group adjacent to nitrogen. Treatment of these intermediates with a Lewis acid in dichloromethane permits the regeneration of a reactive acyliminium ion that is then reacted with a range of nucleophilic species.Entities:
Keywords: N-acyliminium ions; anodic oxidation; diversity-oriented synthesis; heterocycles; lactams
Mesh:
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Year: 2015 PMID: 26371961 PMCID: PMC4629799 DOI: 10.1002/anie.201504775
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336