Issue 0, 1968

Natural acetylenes. Part XXVII. An antifungal acetylenic furanoid keto-ester (wyerone) from shoots of the broad bean (Vicia faba L.; Fam. Papilionaceae)

Abstract

The isolation and determination of the structure of the fungitoxic principle of the broad bean, Vicia faba L., is described. The natural material is the acetylenic keto-ester R[graphic omitted]·CH[graphic omitted]CH·CO2Me (R =cis-EtCH:CH·C⋮C·CO), contaminated with about 2% of the more saturated ketone (R = BuC⋮C·CO). In addition, the alcohol (R =cis-EtCH:CH·C⋮C·CHOH) was found in the shoot extract. These compounds, as well as the lower homologue (R =cis-MeCH:CH·C⋮C·CO), its trans-isomer, the aldehyde (R = OCH·C⋮C), the alcohol (R = HO·CH2·C⋮C), and the close thiophen analogue MeCH[graphic omitted]CH·C⋮C·CO·[graphic omitted]·CH[graphic omitted]CH·CO2Me were synthesised, and their fungitoxic properties were compared.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 2455-2462

Natural acetylenes. Part XXVII. An antifungal acetylenic furanoid keto-ester (wyerone) from shoots of the broad bean (Vicia faba L.; Fam. Papilionaceae)

C. H. Fawcett, D. M. Spencer, R. L. Wain, A. G. Fallis, E. R. H. Jones, M. L. Quan, C. B. Page, V. Thaller, D. C. Shubrook and P. M. Whitham, J. Chem. Soc. C, 1968, 2455 DOI: 10.1039/J39680002455

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