2026-08-29T15:42:49Zhttps://riubu.ubu.es/oai/request

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

00925njm 22002777a 4500 dc Álvarez Manuel, Estela author Miguel, Delia author García García, Patricia author Fernández Rodríguez, Manuel A. author Rodríguez, Félix author Sanz Díez, Roberto author 2012 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 0039-7881 http://hdl.handle.net/10259/3801 10.1055/s-0031-1290950 benzofulvenes catalysis gold indoles tandem reactions Synthesis of 2-Indol-3-ylbenzofulvenes through a Tandem Reaction Catalyzed by Cationic Gold(I) Complexes