Palladium-Catalyzed Site-Selective Hydrogenation of Unactivated Alkenes Directed by 8-Aminoquinoline Amides

Chem Pharm Bull (Tokyo). 2024;72(10):909-912. doi: 10.1248/cpb.c24-00433.

Abstract

We have developed a method for the site-selective hydrogenation of unactivated alkenes using 8-aminoquinoline amide as the directing group. For unactivated alkenes with two C-C double bonds, Daugulis's 8-aminoquinoline amide facilitated the site-selective hydrogenation of the desired C-C double bond, producing a product in which one C-C double bond was reduced. Site-selective reduction methodologies using intramolecular directing groups are expected to contribute significantly to the synthesis of molecules with multiple reducible functional groups in the future.

Keywords: directing group; hydrogenation; hydrosilane; site-selective; unactivated alkene.

MeSH terms

  • Alkenes* / chemical synthesis
  • Alkenes* / chemistry
  • Amides* / chemical synthesis
  • Amides* / chemistry
  • Aminoquinolines* / chemical synthesis
  • Aminoquinolines* / chemistry
  • Catalysis
  • Hydrogenation
  • Molecular Structure
  • Palladium* / chemistry

Substances

  • Alkenes
  • Palladium
  • Amides
  • 8-aminoquinoline
  • Aminoquinolines