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dc.contributor.authorÁlvarez, Eleuterio-
dc.contributor.authorPaneque, Margarita-
dc.contributor.authorLópez Poveda, Manuel-
dc.contributor.authorRendón, Nuria-
dc.date.accessioned2011-05-26T11:27:51Z-
dc.date.available2011-05-26T11:27:51Z-
dc.date.issued2005-12-02-
dc.identifier.citationAngewandte Chemie - International Edition 45(3): 474-477 (2005)es_ES
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10261/36104-
dc.description4 páginas, figuras.es_ES
dc.description.abstractA new synthesis of iridabenzene species involves the coupling of MeCH-CH2 with iridacycles 1 and 2. Surprisingly, the structure of the coupling product of the iridacyclopentadienes with propene (3 or 4) is highly susceptible to the nature of the substituents in the starting metallacycle.es_ES
dc.description.sponsorshipFinancial support from the Spanish Ministerio de Educación y Ciencia (MEC; Projects BQU2001–1995 and CTQ2004-00409/BQU, FEDER support), from the Junta de Andalucía, and from the EU COST Action WG-D17-003 are gratefully acknowledged. N.R. thanks the MEC for a grant.es_ES
dc.language.isoenges_ES
dc.publisherWiley-VCHes_ES
dc.rightsclosedAccesses_ES
dc.subjectAromaticityes_ES
dc.subjectC-C couplinges_ES
dc.subjectIridiumes_ES
dc.subjectMetallabenzeneses_ES
dc.subjectMetallacycleses_ES
dc.titleFormation of Iridabenzenes by Coupling of Iridacyclopentadienes and Alkeneses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1002/anie.200502437-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1002/anie.200502437es_ES
dc.identifier.e-issn1521-3773-
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