The application of molecular tethers in controlling axial chirality

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dc.contributor.authorReen, Michael
dc.contributor.authorO'Sullivan, Timothy P.
dc.date.accessioned2017-06-20T15:50:37Z
dc.date.available2017-06-20T15:50:37Z
dc.date.issued2016-06
dc.date.updated2017-06-20T10:47:13Z
dc.description.abstractAtropisomeric biaryl compounds are an attractive target in organic chemistry due to their abundance in nature and their utility as ligands in catalysis. Among the methods available for their synthesis, the use of chiral tethers offers very high levels of stereocontrol. In this article, we review the application of molecular tethers in controlling axial chirality across a range of different ligands and natural products.en
dc.description.statusPeer revieweden
dc.description.versionAccepted Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationReen, M. and O'Sullivan, Timothy P. (2016) 'The Application of Molecular Tethers in Controlling Axial Chirality'. Mini-Reviews in Organic Chemistry, 13(3), pp. 206-218. doi: 10.2174/1570193X13666160510114626en
dc.identifier.doi10.2174/1570193X13666160510114626
dc.identifier.endpage218en
dc.identifier.issn1570-193X
dc.identifier.issued3en
dc.identifier.journaltitleMini-Reviews in Organic Chemistryen
dc.identifier.startpage206en
dc.identifier.urihttps://hdl.handle.net/10468/4119
dc.identifier.volume13en
dc.language.isoenen
dc.publisherBentham Science Publishersen
dc.rights© 2016 Bentham Science Publishersen
dc.subjectAtropisomeric biaryl compounden
dc.subjectAxial chiralityen
dc.subjectBiarylsen
dc.subjectStereoinductionen
dc.subjectSynthesisen
dc.titleThe application of molecular tethers in controlling axial chiralityen
dc.typeArticle (peer-reviewed)en
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