4.6 Article

Visible-Light Photoredox-Catalyzed Giese Reaction: Decarboxylative Addition of Amino Acid Derived -Amino Radicals to Electron-Deficient Olefins

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 22, Issue 38, Pages 13464-13468

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201602257

Keywords

amino acid; decarboxylation; heterocycles; photoredox catalysis

Funding

  1. European Research Council under the European Union/ERC [617044]
  2. European Research Council (ERC) [617044] Funding Source: European Research Council (ERC)

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A tin- and halide-free, visible-light photoredox-catalyzed Giese reaction was developed. Primary and secondary -amino radicals were generated readily from amino acids in the presence of catalytic amounts of an iridium photocatalyst. The reactivity of the -amino radicals has been evaluated for the functionalization of a variety of activated olefins.

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