Enantioselective Total Synthesis of Andrographolide and 14-Hydroxy-Colladonin: Carbonyl Reductive Coupling and trans-Decalin Formation by Hydrogen Transfer

Angew Chem Int Ed Engl. 2020 Dec 14;59(51):23169-23173. doi: 10.1002/anie.202011363. Epub 2020 Oct 15.

Abstract

An enantioselective total synthesis of the labdane diterpene andrographolide, the bitter principle of the herb Andrographis paniculata (known as "King of Bitters"), was accomplished in 14 steps (LLS). Key transformations include iridium-catalyzed carbonyl reductive coupling to form the quaternary C4 stereocenter, diastereoselective alkene reduction to establish the trans-decalin ring, and carbonylative lactonization to install the α-alkylidene-β-hydroxy-γ-butyrolactone.

Keywords: enantioselectivity; hydrogen transfer; iridium; labdane diterpenoids; total synthesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Andrographis / chemistry
  • Catalysis
  • Coordination Complexes / chemistry
  • Diterpenes / chemical synthesis*
  • Diterpenes / chemistry
  • Hydrogen / chemistry*
  • Molecular Structure
  • Naphthalenes / chemical synthesis*
  • Naphthalenes / chemistry
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • Coordination Complexes
  • Diterpenes
  • Naphthalenes
  • andrographolide
  • Hydrogen
  • decalin