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dc.contributor.authorLevonis, Stephanen_US
dc.contributor.authorBornaghi, Laurenten_US
dc.contributor.authorHouston, Todden_US
dc.date.accessioned2017-04-24T11:09:35Z
dc.date.available2017-04-24T11:09:35Z
dc.date.issued2007en_US
dc.identifier.issn00049425en_US
dc.identifier.doi10.1071/CH07231en_US
dc.identifier.urihttp://hdl.handle.net/10072/17937
dc.description.abstractBoric acid catalyzes the monoesterification of malonic acid, likely through a chelation mechanism that is not available to the monoester product. Under more forcing conditions, diesters form to some extent, but conditions can be optimized to favour the monoester product (56-80%). With the easily handled solid acid catalyst, these reactions can be run with excess alcohol as solvent or with stoichiometric amounts of alcohol in acetonitrile with moderate heating.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_US
dc.languageEnglishen_US
dc.language.isoen_US
dc.publisherCSIRO Publishingen_US
dc.publisher.placeAustraliaen_US
dc.relation.ispartofstudentpublicationYen_US
dc.relation.ispartofpagefrom821en_US
dc.relation.ispartofpageto823en_US
dc.relation.ispartofjournalAustralian Journal of Chemistryen_US
dc.relation.ispartofvolume60en_US
dc.rights.retentionYen_US
dc.subject.fieldofresearchcode250301en_US
dc.titleSelective Monoesterification of Malonic Acid Catalyzed by Boric Aciden_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyOffice of the Snr Dep Vice Chancellor, Institute for Glycomicsen_US
gro.date.issued2015-05-21T05:34:37Z
gro.hasfulltextNo Full Text


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