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Visible-Light-Enabled Direct Decarboxylative N-Alkylation.

Vu T NguyenViet D NguyenGraham C HaugNgan T H VuongHang T DangHadi D ArmanOleg V Larionov
Published in: Angewandte Chemie (International ed. in English) (2020)
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.
Keyphrases
  • visible light
  • drug discovery
  • electron transfer
  • public health
  • risk assessment