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dc.contributor.authorClarke, Matthew L.
dc.contributor.authorJones, Charlotte E. S.
dc.contributor.authorFrance, Marcia B.
dc.date.accessioned2013-12-05T11:31:01Z
dc.date.available2013-12-05T11:31:01Z
dc.date.issued2007-09-14
dc.identifier.citationClarke , M L , Jones , C E S & France , M B 2007 , ' The first organocatalytic carbonyl-ene reaction : isomerisation-free C-C bond formations catalysed by H-bonding thio-ureas ' , Beilstein Journal of Organic Chemistry , vol. 3 , 24 . https://doi.org/10.1186/1860-5397-3-24en
dc.identifier.otherPURE: 623855
dc.identifier.otherPURE UUID: 3f93b7d3-d54a-4f89-97ed-64b7fcb2e02a
dc.identifier.otherWOS: 000252525900001
dc.identifier.otherScopus: 38149081322
dc.identifier.otherORCID: /0000-0002-2444-1244/work/59464630
dc.identifier.urihttps://hdl.handle.net/10023/4267
dc.description.abstractIntramolecular carbonyl ene reactions of highly activated enophiles can be catalysed by H-bonding thio-ureas to give tertiary alcohols in high yields without extensive isomerisation side products. An asymmetric variant of this reaction was realised using a chiral thiourea but was limited by low enantioselectivity (up to 33% e. e.) and low turnover frequencies.
dc.format.extent4
dc.language.isoeng
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
dc.rights© 2007 Clarke et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)en
dc.subjectASYMMETRIC CATALYSISen
dc.subjectCOMPLEXESen
dc.subjectACIDSen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleThe first organocatalytic carbonyl-ene reaction : isomerisation-free C-C bond formations catalysed by H-bonding thio-ureasen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1186/1860-5397-3-24
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=38149081322&partnerID=8YFLogxKen


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