RT info:eu-repo/semantics/article
T1 Solvent- and ligand-induced switch of selectivity in gold(I)-catalyzed tandem reactions of 3-propargylindoles
A1 Álvarez Manuel, Estela
A1 Miguel, Delia
A1 García García, Patricia
A1 Fernández Rodríguez, Manuel A.
A1 Rodríguez, Félix
A1 Sanz Díez, Roberto
K1 catalysis
K1 gold
K1 indoles
K1 Nazarov cyclizations
K1 selectivity
K1 Química orgánica
K1 Chemistry, Organic
AB 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
PB Beilstein-Institut
SN 1860-5397
YR 2011
FD 2011-06
LK http://hdl.handle.net/10259/3799
UL http://hdl.handle.net/10259/3799
LA eng
NO 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.)
DS Repositorio Institucional de la Universidad de Burgos
RD 24-dic-2024