Enantioselective organocatalytic partial transfer hydrogenation of lactone-fused quinolines

Org Lett. 2014 Jun 6;16(11):2982-5. doi: 10.1021/ol5011196. Epub 2014 May 22.

Abstract

The first enantioselective synthesis of 4-aza-podophyllotoxin derivatives by partial transfer hydrogenation of lactone-fused quinolines was achieved using a chiral Brønsted acid catalyst. This reaction was extended to a large scope of substrates with good yields and enantioselectivities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Hydrogenation
  • Lactones / chemical synthesis*
  • Lactones / chemistry
  • Molecular Structure
  • Quinolines / chemical synthesis*
  • Quinolines / chemistry
  • Stereoisomerism

Substances

  • Lactones
  • Quinolines