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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.identifier623855
dc.identifier3f93b7d3-d54a-4f89-97ed-64b7fcb2e02a
dc.identifier000252525900001
dc.identifier38149081322
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.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.format.extent206664
dc.language.isoeng
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
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.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1186/1860-5397-3-24
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=38149081322&partnerID=8YFLogxKen


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