Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5220286 | Tetrahedron | 2011 | 9 Pages |
Abstract
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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Serge R. Banini, Michael R. Turner, Matthew M. Cummings, Björn C.G. Söderberg,