Biosynthesis of ascochitine: incorporation studies with advanced precursors
Abstract
Evidence is presented that the first step of the biosynthesis of ascochitine (1), a metabolite of Ascochyta fabae Speg., involves methylation of a hexaketide, followed by cyclization, reduction to the aldehyde, dehydration, and eventually oxidation of the methyl group at C(7) to a carboxy group.
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