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dc.contributor.authorHe, Zhen; orcid: 0000-0002-8314-2690
dc.contributor.authorPerry, Gregory J P; orcid: 0000-0001-8173-3369
dc.contributor.authorProcter, David J; orcid: 0000-0003-3179-2509
dc.date.accessioned2021-07-16T01:12:00Z
dc.date.available2021-07-16T01:12:00Z
dc.date.issued2020-01-15
dc.identifierpmcid: PMC8150100
dc.identifierdoi: 10.1039/c9sc05668h
dc.identifierpmid: 34123295
dc.identifier.citationChemical science, volume 11, issue 7, page 2001-2005
dc.identifier.urihttp://hdl.handle.net/10034/625271
dc.descriptionFrom Europe PMC via Jisc Publications Router
dc.descriptionHistory: ppub 2020-01-01, epub 2020-01-15
dc.descriptionPublication status: Published
dc.description.abstractA metal-free, oxidative coupling of phenols with various nucleophiles, including arenes, 1,3-diketones and other phenols, is reported. Cross-coupling is mediated by a sulfoxide which inverts the reactivity of the phenol partner. Crucially, the process shows high selectivity for cross-<i>versus</i> homo-coupling and allows efficient access to a variety of aromatic scaffolds including biaryls, benzofurans and, through an iterative procedure, aromatic oligomers.
dc.languageeng
dc.rightsLicence for this article: cc by
dc.sourceissn: 2041-6520
dc.sourceessn: 2041-6539
dc.sourcenlmid: 101545951
dc.titleSulfoxide-mediated oxidative cross-coupling of phenols.
dc.typearticle
dc.date.updated2021-07-16T01:10:29Z


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