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

Authors :
Banini, Serge R.
Turner, Michael R.
Cummings, Matthew M.
Söderberg, Björn C.G.
Source :
Tetrahedron. May2011, Vol. 67 Issue 20, p3603-3611. 9p.
Publication Year :
2011

Abstract

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. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404020
Volume :
67
Issue :
20
Database :
Academic Search Index
Journal :
Tetrahedron
Publication Type :
Academic Journal
Accession number :
60436084
Full Text :
https://doi.org/10.1016/j.tet.2011.03.029