2026-04-29T04:00:31Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/38002021-11-10T09:38:24Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594

Sanjuán Cortázar, Ana María Martínez Cuezva, Alberto García García, Patricia Fernández Rodríguez, Manuel A. Sanz Díez, Roberto 2015-07-27T11:30:48Z 2015-07-27T11:30:48Z 2013-10 1860-5397 http://hdl.handle.net/10259/3800 10.3762/Fbjoc.9.263 The cyclization of o-(alkynyl)-3-(methylbut-2-enyl)benzenes, 1,6-enynes having a condensed aromatic ring at C3–C4 positions, has been studied under the catalysis of cationic gold(I) complexes. The selective 6-endo-dig mode of cyclization observed for the 7-substituted substrates in the presence of water or methanol giving rise to hydroxy(methoxy)-functionalized dihydronaphthalene derivatives is highly remarkable in the context of the observed reaction pathways for the cycloisomerizations of 1,6-enynes bearing a trisubstituted olefin Ministerio de Ciencia e Innovación (MICINN) and FEDER (CTQ2010-15358) application/pdf eng Beilstein-Institut Beilstein Journal of Organic Chemistry, 2013. V. 9, p. 2242–2249 Gold catalysis for organic synthesis II http://dx.doi.org/10.3762/Fbjoc.9.263 info:eu-repo/grantAgreement/FEDER/CTQ2010-15358 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Este documento está sujeto a una licencia de uso Creative Commons, por la cual está permitido hacer copia, distribuir, comunicar públicamente, remezclar, transformar y crear a partir del material para cualquier finalidad, incluso comercial, siempre que se cite al autor original, se proporcione un enlace a la licencia y se indique si se han realizado cambios info:eu-repo/semantics/openAccess catalysis dihydronaphthalenes gold gold catalysis hydroxycyclization selectivity Química orgánica Chemistry, Organic Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion