Lewis acid-mediated displacements of alkoxydioxolanes: synthesis of a 1,2-dioxolane natural product

Org Lett. 1999 Nov 4;1(9):1391-3. doi: 10.1021/ol990954y.

Abstract

[formula: see text] Addition of electron-rich alkenes to the peroxycarbenium ions derived from Lewis acid-mediated ionization of 3-alkoxy-1,2-dioxolanes provides an efficient route for the synthesis of substituted 1,2-dioxolanes. The methodology is illustrated with a rapid synthesis of a 1,2-dioxolane natural product related to the plakinic acids.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acids / chemistry*
  • Dioxolanes / chemistry*

Substances

  • Acids
  • Dioxolanes