| Literature DB >> 32050048 |
Vu T Nguyen1, Viet D Nguyen1, Graham C Haug1, Ngan T H Vuong1, Hang T Dang1, Hadi D Arman1, Oleg V Larionov1.
Abstract
The development of efficient and selective C-N bond-forming reactions from abundant feedstock chemicals remains a central theme in organic chemistry owing to the key roles of amines in synthesis, drug discovery, and materials science. Herein, we present a dual catalytic system for the N-alkylation of diverse aromatic carbocyclic and heterocyclic amines directly with carboxylic acids, by-passing their preactivation as redox-active esters. The reaction, which is enabled by visible-light-driven, acridine-catalyzed decarboxylation, provides access to N-alkylated secondary and tertiary anilines and N-heterocycles. Additional examples, including double alkylation, the installation of metabolically robust deuterated methyl groups, and tandem ring formation, further demonstrate the potential of the direct decarboxylative alkylation (DDA) reaction.Entities:
Keywords: amination; carboxylic acids; copper catalysis; photocatalysis; visible light
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Year: 2020 PMID: 32050048 PMCID: PMC7200280 DOI: 10.1002/anie.201916710
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336