Total Synthesis of Hoiamide A Using an Evans-Tishchenko Reaction as a Key Step

Org Lett. 2019 Jul 19;21(14):5471-5474. doi: 10.1021/acs.orglett.9b01735. Epub 2019 Jul 5.

Abstract

The first total synthesis of neurotoxic cyclodepsipeptide hoiamide A (1) has been accomplished. The synthesis features the use of an Evans-Tishchenko fragment coupling between a five-stereogenic-center-containing β-hydroxyketone and a chiral aldehyde derived from threonine.

Publication types

  • Research Support, Non-U.S. Gov't