Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/136595
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dc.contributor.authorBudwitz, J.E.-
dc.contributor.authorNewton, C.G.-
dc.date.issued2022-
dc.identifier.citationSynlett: accounts and rapid communications in synthetic organic chemistry, 2022; 33(15):1473-1480-
dc.identifier.issn0936-5214-
dc.identifier.issn1437-2096-
dc.identifier.urihttps://hdl.handle.net/2440/136595-
dc.descriptionArticle published online: 27 June 2022-
dc.description.abstractpara-Quinones feature extensively as targets and/or intermediates throughout a number of chemical and biological subdisciplines, highlighting the importance of efficient preparative methods. This Synpacts article provides an overview of ring forming approaches to para-hydroquinones and para-benzoquinones, concluding with our recent contribution concerning the development of 2,5-bis(tert-butyldimethylsilyloxy)furans as vicinal bisketene equivalents in the Diels–Alder reaction.-
dc.description.statementofresponsibilityJessica E. Budwitz, Christopher G. Newton-
dc.language.isoen-
dc.publisherThieme Publishing-
dc.rights© 2022. Thieme. All rights reserved-
dc.source.urihttp://dx.doi.org/10.1055/s-0041-1737966-
dc.subjectDiels–Alder; cycloaddition; annulation; hydroquinone; benzoquinone; furan-
dc.titleRing Forming Approaches to para-Quinones: Toward a General Diels-Alder Disconnection-
dc.typeJournal article-
dc.identifier.doi10.1055/s-0041-1737966-
dc.relation.granthttp://purl.org/au-research/grants/arc/DE180100462-
pubs.publication-statusPublished-
dc.identifier.orcidNewton, C.G. [0000-0002-8962-5917]-
Appears in Collections:Chemistry publications

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