2026-04-29T05:10:30Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/38012025-12-15T08:28:42Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594

Álvarez Manuel, Estela 25 500 Miguel, Delia 368 500 0000-0002-7876-3986 García García, Patricia 0c6817a7-07ab-499f-877c-c534362475cd 500 Fernández Rodríguez, Manuel A. 174 500 0000-0002-0120-5599 Rodríguez, Félix bd204e31-71db-407f-8054-c7acbccad8bf 500 Sanz Díez, Roberto 531 500 0000-0003-2830-0892 2015-07-27T11:46:23Z 2015-07-27T11:46:23Z 2012 0039-7881 http://hdl.handle.net/10259/3801 10.1055/s-0031-1290950 A new access to benzofulvenes bearing an indol-3-yl substituent at C-2 has been developed. Treatment of 3-propargylindoles possessing an additional hydroxy group at the other pro­pargylic position with a cationic gold(I) complex triggers a tandem 1,2-indole migration/aura-iso-Nazarov cyclization/elimination sequence that takes place under mild conditions MICINN (CTQ2010-15358 and CTQ2009-09949), Junta de Castilla y Leon (BU021A09 and GR-172), MEC (FPU predoctoral fellowships to E.A. and D.M.), 'Ramon y Cajal' contract to M.A.F.R., 'Juan de la Cierva' contract to P.G.G. application/pdf eng Thieme Synthesis. 2012, V. 44, n. 12, p. 1874-1884 https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0031-1290950 info:eu-repo/grantAgreement/MICINN/CTQ2010-15358 info:eu-repo/grantAgreement/MICINN/CTQ2009-09949 info:eu-repo/grantAgreement/JCyL/BU021A09 info:eu-repo/grantAgreement/JCyL/GR-172 benzofulvenes catalysis gold indoles tandem reactions Química orgánica Chemistry, Organic Synthesis of 2-Indol-3-ylbenzofulvenes through a Tandem Reaction Catalyzed by Cationic Gold(I) Complexes info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion © Georg Thieme Verlag, Stuttgart·New York info:eu-repo/semantics/openAccess THUMBNAIL Synthesis_2012.pdf.jpg Synthesis_2012.pdf.jpg IM Thumbnail image/jpeg 4371 https://riubu.ubu.es/bitstream/10259/3801/4/Synthesis_2012.pdf.jpg cff8fb6eeac39663f53fe57b41ac867f MD5 4 Alvarez-synthesis_2012.pdf.jpg Alvarez-synthesis_2012.pdf.jpg IM Thumbnail image/jpeg 4371 https://riubu.ubu.es/bitstream/10259/3801/5/Alvarez-synthesis_2012.pdf.jpg cff8fb6eeac39663f53fe57b41ac867f MD5 5 ORIGINAL Alvarez-synthesis_2012.pdf Alvarez-synthesis_2012.pdf application/pdf 622534 https://riubu.ubu.es/bitstream/10259/3801/1/Alvarez-synthesis_2012.pdf 02aa12f84fa704a8fcb4105dfe46a62d MD5 1 LICENSE license.txt license.txt text/plain; charset=utf-8 1362 https://riubu.ubu.es/bitstream/10259/3801/2/license.txt 5d013bfa6e473ff0db22cd82a4d71a70 MD5 2 TEXT Synthesis_2012.pdf.txt Synthesis_2012.pdf.txt Extracted text text/plain 59336 https://riubu.ubu.es/bitstream/10259/3801/3/Synthesis_2012.pdf.txt 71e004b0d9419552f9dc5008d7abbae4 MD5 3 10259/3801 oai:riubu.ubu.es:10259/3801 2025-12-15 09:28:42.188 Repositorio Institucional de la Universidad de Burgos bubrep@ubu.es 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