Total Synthesis of (±)-Grandilodine B

Org Lett. 2017 Apr 7;19(7):1828-1830. doi: 10.1021/acs.orglett.7b00591. Epub 2017 Mar 15.

Abstract

The first total synthesis of the opened-type Kopsia alkaloid grandilodine B is reported. Four stereocenters of this alkaloid, three of them quaternary, are stereoselectively generated by a Diels-Alder reaction, a diastereoselective cyanation of tertiary alcohol, and a facial-selective nitrone 1,3-dipolar cycloaddition.

Publication types

  • Research Support, Non-U.S. Gov't