A one-step synthesis of the depsidone furfuric acid
Date
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
The structurally unique depsidone furfuric acid (1) has been prepared in one step by the acid-catalysed alkylation of methyl β-orsellinate (6) or of atranorin (4) with physodalic acid (7). This mode of synthesis gives credence to the proposal that (1) is an artefact of the isolation procedure rather than a true metabolite of the lichen Pseudevernia furfuracea.
Description
Keywords
Citation
Collections
Source
Australian Journal of Chemistry