The fungitoxicity of substituted 2‐phenylbenzofurans

Thirty-seven 2-phenylbenzofurans, variously substituted in the homocyclic rings, were synthesised and assessed for antifungal activity in laboratory tests. High activity was shown only by compounds containing a hydroxy group, though amino compounds were also fungitoxic but at a lower level. Possible mechanisms by which these substitutions impart fungitoxicity are discussed with particular reference to the partitioning properties of the molecule.