Jump to main content
Jump to site search

Issue 2, 1999
Previous Article Next Article

Julia–Colonna asymmetric epoxidation of furyl styryl ketone as a route to intermediates to naturally-occurring styryl lactones

Abstract

The enone 1 was oxidized stereoselectively using urea-hydrogen peroxide with polyeucine as the catalyst to give the epoxide 2 which was used to make (+)-goniotriol 7, (+)-goniofufurone 8, (+)-8-acetylgonitriol 9 and gonio-pypyrone 10.

Back to tab navigation

Article type: Paper
DOI: 10.1039/A808436J
Citation: J. Chem. Soc., Perkin Trans. 1, 1999,0, 103-106
  •   Request permissions

    Julia–Colonna asymmetric epoxidation of furyl styryl ketone as a route to intermediates to naturally-occurring styryl lactones

    W. Chen and S. M. Roberts, J. Chem. Soc., Perkin Trans. 1, 1999, 0, 103
    DOI: 10.1039/A808436J

Search articles by author

Spotlight

Advertisements