A Convenient Method for the Synthesis of Dehydroquinic Acid

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dc.contributor.authorLe Sann, C.
dc.contributor.authorAbell, C.
dc.contributor.authorAbell, A.
dc.date.issued2003
dc.description.abstractA convenient synthesis of dehydroquinic acid and its corresponding methyl ester are described. Protection of the trans diol of quinic acid, followed by PCC oxidation, gave fully protected dehydroquinic acid. This gave methyl dehydroquinate on mild acid catalyzed hydrolysis. Ester hydrolysis then gave potassium dehydroquinate which was treated with amberlite to afford dehydroquinic acid.
dc.description.statementofresponsibilityChristine Le Sann; Chris Abell; Andrew D. Abell
dc.identifier.citationSynthetic Communications: an international journal for rapid communication of synthetic organic chemistry, 2003; 33(4):527-533
dc.identifier.doi10.1081/SCC-120015805
dc.identifier.issn0039-7911
dc.identifier.issn1532-2432
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]
dc.identifier.urihttp://hdl.handle.net/2440/34470
dc.language.isoen
dc.publisherMarcel Dekker Inc
dc.source.urihttps://doi.org/10.1081/scc-120015805
dc.subjectShikimate pathway
dc.subjectDehydroquinic acid
dc.subjectSynthesis
dc.subjectSelective protection
dc.titleA Convenient Method for the Synthesis of Dehydroquinic Acid
dc.typeJournal article
pubs.publication-statusPublished

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