4.5 Article

Enantioselective C-H Alkylation of N-Arylbenzamides with Vinyl Ethers Catalyzed by an Iridium/Chiral Phosphoramidite-Olefin Complex

Journal

SYNTHESIS-STUTTGART
Volume 54, Issue 21, Pages 4753-4763

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/a-1672-6284

Keywords

enantioselectivity; iridium; benzamides; catalysis; C-H activation

Funding

  1. Japan Society for the Promotion of Science (JSPS) KAKENHI [JP19H02721, JP20J23499]
  2. JSPS

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Chiral phosphoramidite-olefin hybrid ligands were effective in the iridium-catalyzed asymmetric alkylation of N-arylbenzamides with vinyl ethers. The reaction yield was high, with high branch selectivity and enantioselectivity.
Chiral phosphoramidite-olefin hybrid ligands were found to be effective in the iridium-catalyzed asymmetric alkylation of N-arylbenzamides with vinyl ethers. The reaction is catalyzed by a hydroxo-iridium catalyst coordinated with the hybrid ligand to give the corresponding products in high yields with high branch selectivity and enantioselectivity.

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