Palladium-catalyzed synthesis of cephalotaxine analogues

Chemistry. 2000 Feb 4;6(3):510-8. doi: 10.1002/(sici)1521-3765(20000204)6:3<510::aid-chem510>3.0.co;2-h.

Abstract

The synthesis of cephalotaxine ring analogues 10 was achieved by two successive intramolecular palladium-catalyzed reactions of 12 via 11, namely an allylic amination and a Heck reaction. The substrates 12 were obtained by alkylation of primary amines 13 with tosylates 14.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Catalysis
  • Harringtonines / chemical synthesis*
  • Homoharringtonine
  • Palladium*

Substances

  • Harringtonines
  • Palladium
  • Homoharringtonine