2024-03-28T12:45:10Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/37992021-11-10T09:38:24Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594
Álvarez Manuel, Estela
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500
Miguel, Delia
368
500
García García, Patricia
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500
Fernández Rodríguez, Manuel A.
174
500
Rodríguez, Félix
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500
Sanz Díez, Roberto
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500
2015-07-27T09:55:12Z
2015-07-27T09:55:12Z
2011-06
1860-5397
http://hdl.handle.net/10259/3799
10.3762/bjoc.7.89
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
MICINN (CTQ2010-15358 and CTQ2009-09949), Junta de Castilla y Leon (BU021A09 and GR-172), MEC (FPU predoctoral fellowship to D.M.), Ramón y Cajal (contract to M.A F R.), Juan de la Cierva (contract to P.G.G.)
application/pdf
eng
Beilstein-Institut
Beilstein Journal of Organic Chemistry. 2011, v. 7, p. 786–793
Gold catalysis for organic synthesis
http://dx.doi.org/10.3762/bjoc.7.89
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
Attribution 4.0 International
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info:eu-repo/semantics/openAccess
catalysis
gold
indoles
Nazarov cyclizations
selectivity
Química orgánica
Chemistry, Organic
Solvent- and ligand-induced switch of selectivity in gold(I)-catalyzed tandem reactions of 3-propargylindoles
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
CC-LICENSE
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oai:riubu.ubu.es:10259/3799
2021-11-10 10:38:24.367
Repositorio Institucional de la Universidad de Burgos
bubrep@ubu.es
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