2026-06-30T01:11:28Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/38012025-12-15T08:28:42Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594
Synthesis of 2-Indol-3-ylbenzofulvenes through a Tandem Reaction Catalyzed by Cationic Gold(I) Complexes
Álvarez Manuel, Estela
Miguel, Delia
García García, Patricia
Fernández Rodríguez, Manuel A.
Rodríguez, Félix
Sanz Díez, Roberto
benzofulvenes
catalysis
gold
indoles
tandem reactions
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
2015-07-27
2015-07-27
2012
info:eu-repo/semantics/article
0039-7881
http://hdl.handle.net/10259/3801
10.1055/s-0031-1290950
eng
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
© Georg Thieme Verlag, Stuttgart·New York
info:eu-repo/semantics/openAccess
Thieme