2026-08-29T14:42:58Zhttps://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 Miguel, Delia García García, Patricia Fernández Rodríguez, Manuel A. Rodríguez, Félix Sanz Díez, Roberto 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