Jump to main content
Jump to site search

Issue 8, 1999
Previous Article Next Article

Total synthesis of the polyenoyltetramic acid mycotoxin erythroskyrine<img border='0' src='http://www.rsc.org/images/entities/h2_char_200a.gif' alt=' '/>†

Abstract

The first total synthesis of erythroskyrine, a polyenoyltetramic acid mycotoxin and principal pigment of Penicillium Islandicum Sopp., is described using a palladium(II) catalysed oxycarbonylation to create the furan-derived bicyclic portion 3 and the phosphonate ester 5 to furnish both the polyenoyl chain and the N-methyl(S )-valine derived tetramic acid terminus.

Back to tab navigation

Article type: Paper
DOI: 10.1039/A809823I
Citation: J. Chem. Soc., Perkin Trans. 1, 1999, 839-842
  •   Request permissions

    Total synthesis of the polyenoyltetramic acid mycotoxin erythroskyrine<img border='0' src='http://www.rsc.org/images/entities/h2_char_200a.gif' alt=' '/>†

    D. J. Dixon, S. V. Ley, T. Gracza and P. Szolcsanyi, J. Chem. Soc., Perkin Trans. 1, 1999, 839
    DOI: 10.1039/A809823I

Search articles by author

Spotlight

Advertisements