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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/124648
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dc.contributor.authorPatel, H.D.-
dc.contributor.authorTran, T.-H.-
dc.contributor.authorSumby, C.J.-
dc.contributor.authorPašteka, L.F.-
dc.contributor.authorFallon, T.-
dc.date.issued2020-
dc.identifier.citationJournal of the American Chemical Society, 2020; 142(8):3680-3685-
dc.identifier.issn0002-7863-
dc.identifier.issn1520-5126-
dc.identifier.urihttp://hdl.handle.net/2440/124648-
dc.description.abstractBoronate ester bullvalenes are now accessible in two to four operationally simple steps. This unlocks late-stage diversification through Suzuki cross-coupling reactions to give mono-, di-, and trisubstituted bullvalenes. Moreover, a linchpin strategy enables preprogrammed installation of two different substituents. Analysis of solution phase isomer distributions and single-crystal X-ray structures reveals that isomer preference in the crystal lattice is due to general shape selectivity.-
dc.description.statementofresponsibilityHarshal D. Patel, Thanh-Huyen Tran, Christopher J. Sumby, Lukáš F. Pašteka, Thomas Fallon-
dc.language.isoen-
dc.publisherAmerican Chemical Society-
dc.rights© 2020 American Chemical Society-
dc.source.urihttp://dx.doi.org/10.1021/jacs.9b12930-
dc.titleBoronate Ester Bullvalenes-
dc.typeJournal article-
dc.identifier.doi10.1021/jacs.9b12930-
dc.relation.granthttp://purl.org/au-research/grants/arc/LE0989336-
pubs.publication-statusPublished-
dc.identifier.orcidPatel, H.D. [0000-0003-1900-0505]-
dc.identifier.orcidSumby, C.J. [0000-0002-9713-9599]-
dc.identifier.orcidFallon, T. [0000-0002-6495-5282]-
Appears in Collections:Aurora harvest 8
Chemistry publications

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