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Updated: Feb 20, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Total Synthesis of the Sesquiterpenoid Periconianone A Based on a Postulated Biogenesis
Raphael Liffert1, Anthony Linden1, Karl Gademann1
1Department of Chemistry, University of Zurich , Winterthurerstrasse 190, Zurich CH 8057, Switzerland.
Abstract:
The first enantioselective total synthesis of the complex tricarbocyclic sesquiterpenoid periconianone A based on a postulated biogenesis is reported. Key elements of the synthetic route include the use of an isopropenyl group as a removable directing group for stereoselective synthesis, a sequence featuring a Rh-mediated O-H insertion/[3,3]-sigmatropic rearrangement and subsequent α-ketol rearrangement, and a late stage aldol reaction to furnish the complex cage-like framework.
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