Stable N-heterocyclic carbene (NHC)-palladium(0) complexes as active catalysts for olefin cyclopropanation reactions with ethyl diazoacetate
| dc.contributor.author | Martín, Carmen | |
| dc.contributor.author | Molina González, Francisco | |
| dc.contributor.author | Álvarez, Eleuterio | |
| dc.contributor.author | Rodríguez Belderraín, Tomás | |
| dc.date.accessioned | 2016-01-13T12:26:07Z | |
| dc.date.available | 2016-01-13T12:26:07Z | |
| dc.date.issued | 2011 | |
| dc.description.abstract | The Pd(0) complexes NHCPdLn (NHC = N-heterocyclic carbene ligand; L = styrene for n = 2 or PR3 for n = 1) efficiently catalyze the olefin cyclopropanation using ethyl diazoacetate (EDA) as the carbene source with activities that improve any other previous described catalytic system based on this metal. Mechanistic studies have shown that all those catalyst precursors deliver in solution the same catalytic species (IPr)Pd(sty), a 14e, unsaturated intermediate that further reacts with EDA to afford (IPr)Pd(=CHCO2Et)(sty), from which cyclopropane is formed. | en_US |
| dc.description.center | CIQSO | |
| dc.description.department | Ingeniería Química, Química Física y Ciencias de los Materiales | |
| dc.description.sponsorship | We thank Prof. P.J. Perez (Univ. Huelva) for helpful and constructive comments on these studies. We thank the Ministerio de Ciencia e Innovacion (grants CTQ2008-00042BQU and CTQ2011-24502) and the Junta de Andalucia (Proyecto P07-FQM-02794) for financial support. CM thanks the MEC for a research fellowship.We thank Prof. P. J. Pérez (Univ. Huelva) for helpful and constructive comments on these studies. We thank the Ministerio de Ciencia e Innovación (grants CTQ2008–00042BQU and CTQ2011–24502) and the Junta de Andalucía (Proyecto P07-FQM-02794) for financial support. CM thanks the MEC for a research fellowship | |
| dc.identifier.citation | Martín, C., Molina, F., Álvarez, E., Rodríguez Belderraín, T.: "Stable N-heterocyclic carbene (NHC)-palladium(0) complexes as active catalysts for olefin cyclopropanation reactions with ethyl diazoacetate". Chemistry - A European Journal. Vol. 17, n. 52, págs. 14885–14895, (2011). DOI: 10.1002/chem.201102900 | en_US |
| dc.identifier.doi | 10.1002/chem.201102900 | |
| dc.identifier.issn | 0947-6539 | |
| dc.identifier.issn | 1521-3765 (electrónico) | |
| dc.identifier.uri | http://hdl.handle.net/10272/11567 | |
| dc.language.iso | eng | en_US |
| dc.publisher | Wiley-VCH Verlag | en_US |
| dc.relation.projectID | info:eu-repo/grantAgreement/Ministerio de Ciencia e Innovacion [CTQ2008-00042BQU, CTQ2011-24502] | |
| dc.relation.projectID | info:eu-repo/grantAgreement/Junta de Andalucia [P07-FQM-02794] | |
| dc.rights | Atribución-NoComercial-SinDerivadas 3.0 España | * |
| dc.rights.accessRights | open access | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/es/ | * |
| dc.subject.other | Diazoester | en_US |
| dc.subject.other | Cyclopropanation | en_US |
| dc.subject.other | Homogeneous catalysis | en_US |
| dc.subject.other | Palladium | en_US |
| dc.title | Stable N-heterocyclic carbene (NHC)-palladium(0) complexes as active catalysts for olefin cyclopropanation reactions with ethyl diazoacetate | en_US |
| dc.type | journal article | en_US |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | d6bc61d2-982b-4854-8502-ab8acb1d525d | |
| relation.isAuthorOfPublication | 44ec727a-e9d0-466d-97eb-2c54fb56986f | |
| relation.isAuthorOfPublication.latestForDiscovery | d6bc61d2-982b-4854-8502-ab8acb1d525d |
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