2026-04-17T12:03:48Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/37992021-11-10T09:38:24Zcom_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 2011-06 The selectivity of our previously described gold-catalyzed tandem reaction, 1,2-indole migration followed by aura-iso-Nazarov cyclization, of 3-propargylindoles bearing (hetero)aromatic substituents at both the propargylic and terminal positions, was reversed by the proper choice of the catalyst and the reaction conditions. Thus, 3-(inden-2-yl)indoles, derived from an aura-Nazarov cyclization (instead of an aura-iso-Nazarov cyclization), were obtained in moderate to good yields from a variety of 3-propargylindoles application/pdf http://hdl.handle.net/10259/3799 eng Beilstein-Institut Solvent- and ligand-induced switch of selectivity in gold(I)-catalyzed tandem reactions of 3-propargylindoles info:eu-repo/semantics/article TEXT RIUBU. Repositorio Institucional de la Universidad de Burgos Hispana