Chemodivergent Metathesis of Dienynes Catalyzed by Ruthenium–Indenylidene Complexes: An Experimental and Computational Study |
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Authors: | Hervé Clavier Dr. Andrea Correa Dr. Eduardo C. Escudero‐Adán Jordi Benet‐Buchholz Dr. Luigi Cavallo Prof. Dr. Steven P. Nolan Prof. Dr. |
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Affiliation: | 1. School of Chemistry, University of St‐Andrews, North Haugh, St Andrews, KY16 9ST (UK), Fax: (+44)?01334‐463808;2. Institute of Chemical Research of Catalonia (ICIQ), Av. Pa?sos Catalans 16, 43007 Tarragona (Spain);3. Dipartmento of Chimica, Universitá di Salerno, Via Salvador Allende, Baronissi (SA), 84081 (Italy), Fax: (+39)?089‐969603 |
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Abstract: | A study on the enyne metathesis reaction leading to the formation cyclic compounds using ruthenium–indenylidene complexes is presented. Several 1,11‐dien‐6‐ynes have been subjected to ruthenium metathesis cyclization by using ruthenium–indenylidene complexes bearing various phosphine and N‐heterocyclic carbene (NHC) ligands. Interestingly, for some substrates chemodivergent metathesis occurs and is a function of the catalyst employed. This led us to investigate the competing “ene‐then‐yne” or “yne‐then‐ene” reaction pathways apparently at play in these systems using both experimental observations and DFT calculations. Experimental and computational studies were found in good agreement and permit to conclude that for phosphine‐containing catalysts, the “ene‐then‐yne” pathway is exclusively adopted. On the other hand, for catalysts bearing NHC ligands, both pathways are possible. |
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Keywords: | density functional calculations enynes homogeneous catalysis metathesis N‐heterocyclic carbenes ruthenium |
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