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A valuable upgrade to the portfolio of cycloaddition reactions

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dc.contributor.authorWalton, John C.
dc.date.accessioned2017-05-02T23:33:53Z
dc.date.available2017-05-02T23:33:53Z
dc.date.issued2016-06-09
dc.identifier.citationWalton , J C 2016 , ' A valuable upgrade to the portfolio of cycloaddition reactions ' , Angewandte Chemie International Edition , vol. 55 , no. 25 , pp. 7034-7036 . https://doi.org/10.1002/anie.201602891en
dc.identifier.issn1521-3773
dc.identifier.otherPURE: 243626246
dc.identifier.otherPURE UUID: e1720ea7-2271-48f6-bab4-3b97abda15b7
dc.identifier.otherBibtex: urn:7da59a6f7fcf77529c77668ac0a13019
dc.identifier.otherScopus: 84973926517
dc.identifier.otherORCID: /0000-0003-2746-6276/work/56638818
dc.identifier.otherWOS: 000382790600001
dc.identifier.urihttps://hdl.handle.net/10023/10696
dc.descriptionThe author thanks EaStCHEM for financial support.en
dc.description.abstractRecently Antonchick and Manna described a unique annulation that knits together three acetophenones to construct cyclopropanes. The cascade is mediated by organo-copper and free radical species and amounts to the first known [1+1+1] cyclotrimerization. It works well for ketones having electron-deficient or electron-rich substituents in their aryl rings.
dc.format.extent3
dc.language.isoeng
dc.relation.ispartofAngewandte Chemie International Editionen
dc.rights© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://dx.doi.org/10.1002/anie.201602891en
dc.subjectCarbocyclesen
dc.subjectCopperen
dc.subjectCyclotrimerizationen
dc.subjectRadicalsen
dc.subjectSynthetic methodsen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleA valuable upgrade to the portfolio of cycloaddition reactionsen
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1002/anie.201602891
dc.description.statusPeer revieweden
dc.date.embargoedUntil2017-05-02


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