Litcius/Paper detail

Enantioselective Total Synthesis of Andrographolide and 14‐Hydroxy‐Colladonin: Carbonyl Reductive Coupling and <i>trans</i>‐Decalin Formation by Hydrogen Transfer

Lin Yang, Thomas Wurm, Binit Sharma Poudel, Michael J. Krische

2020Angewandte Chemie International Edition27 citationsDOIOpen Access PDF

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.

Topics & Concepts

Enantioselective synthesisDecalinTotal synthesisStereocenterChemistryStereochemistryTransfer hydrogenationLabdaneAndrographolideDiterpeneRing (chemistry)KetoneOrganic chemistryCatalysisRutheniumAndrographolide Research and ApplicationsTraditional and Medicinal Uses of AnnonaceaeAlkaloids: synthesis and pharmacology