Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/124648
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dc.contributor.author | Patel, H.D. | - |
dc.contributor.author | Tran, T.-H. | - |
dc.contributor.author | Sumby, C.J. | - |
dc.contributor.author | Pašteka, L.F. | - |
dc.contributor.author | Fallon, T. | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Journal of the American Chemical Society, 2020; 142(8):3680-3685 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.issn | 1520-5126 | - |
dc.identifier.uri | http://hdl.handle.net/2440/124648 | - |
dc.description.abstract | Boronate 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.statementofresponsibility | Harshal D. Patel, Thanh-Huyen Tran, Christopher J. Sumby, Lukáš F. Pašteka, Thomas Fallon | - |
dc.language.iso | en | - |
dc.publisher | American Chemical Society | - |
dc.rights | © 2020 American Chemical Society | - |
dc.source.uri | http://dx.doi.org/10.1021/jacs.9b12930 | - |
dc.title | Boronate Ester Bullvalenes | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1021/jacs.9b12930 | - |
dc.relation.grant | http://purl.org/au-research/grants/arc/LE0989336 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Patel, H.D. [0000-0003-1900-0505] | - |
dc.identifier.orcid | Sumby, C.J. [0000-0002-9713-9599] | - |
dc.identifier.orcid | Fallon, T. [0000-0002-6495-5282] | - |
Appears in Collections: | Aurora harvest 8 Chemistry publications |
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