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Extending the utility of [Pd(NHC)(cinnamyl)Cl] precatalysts : Direct arylation of heterocycles
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dc.contributor.author | Martin, Anthony | |
dc.contributor.author | Chartoire, Anthony Raymond Georges | |
dc.contributor.author | Slawin, Alexandra Martha Zoya | |
dc.contributor.author | Nolan, Steven Patrick | |
dc.date.accessioned | 2012-11-20T16:31:02Z | |
dc.date.available | 2012-11-20T16:31:02Z | |
dc.date.issued | 2012-09-27 | |
dc.identifier.citation | Martin , A , Chartoire , A R G , Slawin , A M Z & Nolan , S P 2012 , ' Extending the utility of [Pd(NHC)(cinnamyl)Cl] precatalysts : Direct arylation of heterocycles ' , Beilstein Journal of Organic Chemistry , vol. 8 , pp. 1637-1643 . https://doi.org/10.3762/bjoc.8.187 | en |
dc.identifier.issn | 1860-5397 | |
dc.identifier.other | PURE: 30087527 | |
dc.identifier.other | PURE UUID: 3794011c-ed1b-4b89-8c9c-9e3f721b15f1 | |
dc.identifier.other | WOS: 000309591800001 | |
dc.identifier.other | Scopus: 84867219499 | |
dc.identifier.other | ORCID: /0000-0002-9527-6418/work/56861423 | |
dc.identifier.uri | https://hdl.handle.net/10023/3257 | |
dc.description.abstract | The use of [Pd(NHC)(cinnamyl)Cl] precatalysts in the direct arylation of heterocycles has been investigated. Among four different precatalysts, [Pd(SIPr)(cinnamyl)Cl] proved to be the most efficient promoter of the reaction. The C–H functionalization of sulfuror nitrogen-containing heterocycles has been achieved at low catalyst loadings. These catalyst charges range from 0.1 to 0.01 mol % palladium. | |
dc.format.extent | 7 | |
dc.language.iso | eng | |
dc.relation.ispartof | Beilstein Journal of Organic Chemistry | en |
dc.rights | © 2012 Martin 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.subject | C-H functionalization | en |
dc.subject | Direct arylation | en |
dc.subject | Heterocycles | en |
dc.subject | N-heterocyclic | en |
dc.subject | Carbenes | en |
dc.subject | Palladium | en |
dc.subject | QD Chemistry | en |
dc.subject.lcc | QD | en |
dc.title | Extending the utility of [Pd(NHC)(cinnamyl)Cl] precatalysts : Direct arylation of heterocycles | en |
dc.type | Journal article | en |
dc.contributor.sponsor | EPSRC | en |
dc.description.version | Publisher PDF | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | https://doi.org/10.3762/bjoc.8.187 | |
dc.description.status | Peer reviewed | en |
dc.identifier.grantnumber | EP/J011053/1 | en |
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