Transition metal-free cascade reactions of alkynols to afford isoquinolin-1(2H)-one and dihydroisobenzofuran derivatives

J Org Chem. 2014 May 16;79(10):4602-14. doi: 10.1021/jo5006312. Epub 2014 Apr 30.

Abstract

Transition metal-free cascade reactions of alkynols with imines have been achieved using potassium tert-butoxide as catalyst. Switching the reaction solvent gives two kinds of products in good yield: isoquinolin-1(2H)-one derivatives and dihydroisobenzofuran derivatives. This approach was used to generate the natural product 8-oxypseudopalmatine in a two-step procedure from commercially available starting materials. Additionally, multicomponent reactions of alkynols, aldehydes, and amines were also successfully achieved to afford isoquinolin-1(2H)-one derivatives.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry*
  • Amines / chemical synthesis*
  • Amines / chemistry
  • Benzofurans / chemistry*
  • Berberine Alkaloids / chemical synthesis*
  • Berberine Alkaloids / chemistry
  • Catalysis
  • Isoquinolines / chemistry*
  • Molecular Structure
  • Transition Elements / chemistry*

Substances

  • 8-oxypseudopalmatine
  • Aldehydes
  • Amines
  • Benzofurans
  • Berberine Alkaloids
  • Isoquinolines
  • Transition Elements