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https://hdl.handle.net/2440/136595
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DC Field | Value | Language |
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dc.contributor.author | Budwitz, J.E. | - |
dc.contributor.author | Newton, C.G. | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Synlett: accounts and rapid communications in synthetic organic chemistry, 2022; 33(15):1473-1480 | - |
dc.identifier.issn | 0936-5214 | - |
dc.identifier.issn | 1437-2096 | - |
dc.identifier.uri | https://hdl.handle.net/2440/136595 | - |
dc.description | Article published online: 27 June 2022 | - |
dc.description.abstract | para-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.statementofresponsibility | Jessica E. Budwitz, Christopher G. Newton | - |
dc.language.iso | en | - |
dc.publisher | Thieme Publishing | - |
dc.rights | © 2022. Thieme. All rights reserved | - |
dc.source.uri | http://dx.doi.org/10.1055/s-0041-1737966 | - |
dc.subject | Diels–Alder; cycloaddition; annulation; hydroquinone; benzoquinone; furan | - |
dc.title | Ring Forming Approaches to para-Quinones: Toward a General Diels-Alder Disconnection | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1055/s-0041-1737966 | - |
dc.relation.grant | http://purl.org/au-research/grants/arc/DE180100462 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Newton, C.G. [0000-0002-8962-5917] | - |
Appears in Collections: | Chemistry publications |
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