The application of molecular tethers in controlling axial chirality

Show simple item record Reen, Michael O'Sullivan, Timothy P. 2017-06-20T15:50:37Z 2017-06-20T15:50:37Z 2016-06
dc.identifier.citation Reen, 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: 10.2174/1570193X13666160510114626 en
dc.identifier.volume 13 en
dc.identifier.issued 3 en
dc.identifier.startpage 206 en
dc.identifier.endpage 218 en
dc.identifier.issn 1570-193X
dc.identifier.doi 10.2174/1570193X13666160510114626
dc.description.abstract Atropisomeric 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.format.mimetype application/pdf en
dc.language.iso en en
dc.publisher Bentham Science Publishers en
dc.rights © 2016 Bentham Science Publishers en
dc.subject Atropisomeric biaryl compound en
dc.subject Axial chirality en
dc.subject Biaryls en
dc.subject Stereoinduction en
dc.subject Synthesis en
dc.title The application of molecular tethers in controlling axial chirality en
dc.type Article (peer-reviewed) en
dc.internal.authorcontactother Tim O'Sullivan, School Of Pharmacy, University College Cork, Cork, Ireland. +353-21-490-3000 Email: en
dc.internal.availability Full text available en 2017-06-20T10:47:13Z
dc.description.version Accepted Version en
dc.internal.rssid 351463690
dc.description.status Peer reviewed en
dc.identifier.journaltitle Mini-Reviews in Organic Chemistry en
dc.internal.copyrightchecked Yes en
dc.internal.licenseacceptance Yes en
dc.internal.IRISemailaddress en

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