2026-04-28T10:08:01Zhttps://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 521 500 Martínez Cuezva, Alberto 344 500 García García, Patricia 0c6817a7-07ab-499f-877c-c534362475cd 500 Fernández Rodríguez, Manuel A. 174 500 Sanz Díez, Roberto 531 500 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 CC-LICENSE license_rdf license_rdf application/rdf+xml; charset=utf-8 908 https://riubu.ubu.es/bitstream/10259/3800/8/license_rdf 0175ea4a2d4caec4bbcc37e300941108 MD5 8 THUMBNAIL Beilstein_J._Org._Chem._2013.pdf.jpg Beilstein_J._Org._Chem._2013.pdf.jpg IM Thumbnail image/jpeg 4481 https://riubu.ubu.es/bitstream/10259/3800/7/Beilstein_J._Org._Chem._2013.pdf.jpg 314ecf814001be42e29f7471405d061c MD5 7 ORIGINAL Beilstein_J._Org._Chem._2013.pdf Beilstein_J._Org._Chem._2013.pdf application/pdf 377733 https://riubu.ubu.es/bitstream/10259/3800/1/Beilstein_J._Org._Chem._2013.pdf cb63d986c1b4b4e8ba9e5319532def17 MD5 1 LICENSE license.txt license.txt text/plain; charset=utf-8 1362 https://riubu.ubu.es/bitstream/10259/3800/5/license.txt 5d013bfa6e473ff0db22cd82a4d71a70 MD5 5 TEXT Beilstein_J._Org._Chem._2013.pdf.txt Beilstein_J._Org._Chem._2013.pdf.txt Extracted text text/plain 26066 https://riubu.ubu.es/bitstream/10259/3800/6/Beilstein_J._Org._Chem._2013.pdf.txt 3a59997d2ecc81222a878bd5e1aad7be MD5 6 10259/3800 oai:riubu.ubu.es:10259/3800 2021-11-10 10:38:24.424 Repositorio Institucional de la Universidad de Burgos bubrep@ubu.es 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