Synthesis of Atisine, Ajaconine, Denudatine, and Hetidine Diterpenoid Alkaloids by a Bioinspired Approach

Angew Chem Int Ed Engl. 2016 Dec 12;55(50):15667-15671. doi: 10.1002/anie.201609882. Epub 2016 Nov 17.

Abstract

A unified approach to four different (atisine, ajaconine, denudatine, and hetidine) diterpenoid alkaloid skeletons was developed and applied to the total synthesis of the natural products dihydroajaconine (2, atisine type) and gymnandine (4, denudatine type). The synthesis features a biogenetically inspired strategy that relies on C-H oxidation, aza-pinacol coupling, and aza-Prins cyclization as key steps.

Keywords: alkaloids; biomimetic synthesis; cyclization; terpenoids; total synthesis.

Publication types

  • Research Support, Non-U.S. Gov't