Coinage Metal-Catalyzed Asymmetric Reactions of ortho-Alkynylaryl and Heteroaryl Aldehydes and Ketones

Molecules. 2022 Oct 17;27(20):6970. doi: 10.3390/molecules27206970.

Abstract

Coinage metals have become the metal of choice due to their excellent catalytic activity in organic transformation processes. Combining various chiral ligands and coinage metals became a productive area of research and access to heterocyclic derivatives according to an efficient and sustainable manner. This review was devoted to the various recently developed coinage metal-catalyzed domino processes of ortho-alkynylaryl and heteroaryl aldehydes and ketones leading to functionalized heterocycles. Various gold chiral complexes were presented, and methods of preparations of chromenes along with indoles were covered. Ag-chiral complexes are also prone to interesting activities such as cyclization followed by reduction and functionalization with enolizable ketones or (diazomethyl)phosphonate. Asymmetric Cu-catalyzed domino cyclization and asymmetric transfer hydrogenation reactions efficiently led to functionalized chromenes. Some remarkable examples involving copper associated with ruthenium in the context of a cyclization and asymmetric hydrogenation process were also presented.

Keywords: asymmetric catalysis; coinage metals; copper; gold; isochromenes; silver.

Publication types

  • Review

MeSH terms

  • Aldehydes
  • Benzopyrans
  • Catalysis
  • Copper
  • Gold
  • Indoles
  • Ketones
  • Organophosphonates*
  • Ruthenium*

Substances

  • Ketones
  • Aldehydes
  • Ruthenium
  • Copper
  • Gold
  • Benzopyrans
  • Indoles
  • Organophosphonates