4.5 Article

Asymmetric Organocatalysis and Photoredox Catalysis for the -Functionalization of Tetrahydroisoquinolines

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2018, Issue 10, Pages 1277-1280

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201800117

Keywords

Cyclic ketones; Tetrahydroisoquinolines; Organocatalysis; Photocatalysis; Alkylation

Funding

  1. Chinese Scholarship Council
  2. European Research Council under the European Union's Seventh Framework Programme (FP)/ ERC Grant [617044]

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The asymmetric -alkylation of tetrahydroisoquinolines with cyclic ketones has been accomplished in the presence of a combined catalytic system consisting of a visible-light photoredox catalyst and a chiral primary amine organocatalyst. The desired products were obtained in good yields, high enantioselectivity, and good to excellent diastereoselectivity. (PC: photoredox cycle, EN: enamine cycle).

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