Total synthesis of (-)-4-desacetoxy-1-oxovindoline: Single atom exchange of an embedded core heteroatom in vindoline

Tetrahedron. 2021 May 7:87:132117. doi: 10.1016/j.tet.2021.132117. Epub 2021 Mar 29.

Abstract

A concise total synthesis of (-)-4-desacetoxy-1-oxovindoline is disclosed, bearing a single heteroatom exchange in the core structure of the natural product 4-desacetoxyvindoline. Central to the synthesis is powerful oxadiazole intramolecular [4+2]/[3+2] cycloaddition cascade that formed four C-C bonds, created three new rings, and established five contiguous stereocenters about the new formed central 6-membered ring.

Keywords: Vinca alkaloids; oxadiazole cycloaddition cascade; vindoline analogue.