A base-modulated chemoselective synthesis of 3-cyanoindoles or 4-cyanoquinolines using a palladium-catalyzed N-heterocyclization

A selective methodology for the synthesis of either 3-cyanoindoles or 4-cyanoquinolines via a base-modulated palladium-catalyzed reductive N-heterocyclization from a common 1-cyano-1-(2-nitrophenyl)-1-alkene precursor is described. The required starting materials were prepared either by a Kosugi–Mig...

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Veröffentlicht in:Tetrahedron 2011-05, Vol.67 (20), p.3603-3611
Hauptverfasser: Banini, Serge R., Turner, Michael R., Cummings, Matthew M., Söderberg, Björn C.G.
Format: Artikel
Sprache:eng
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Zusammenfassung:A selective methodology for the synthesis of either 3-cyanoindoles or 4-cyanoquinolines via a base-modulated palladium-catalyzed reductive N-heterocyclization from a common 1-cyano-1-(2-nitrophenyl)-1-alkene precursor is described. The required starting materials were prepared either by a Kosugi–Migita–Stille coupling of 2-halo-1-nitrobenzenes with a tributyl(1-alkenyl)stannane or by a vicarious nucleophilic substitution (VNS) of nitrobenzenes followed by a Knoevenagel condensation with an aldehyde. [Display omitted]
ISSN:0040-4020
1464-5416
DOI:10.1016/j.tet.2011.03.029