Journal of the American Chemical Society · 2008 · 726 citations · 30 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryCatalyst DesignCatalyst PreparationCatalytic MaterialsCross-coupling ReactionsHeterocycle SynthesisOrganic SynthesisAlkyne MetathesisIndole ChemistryIndole DerivativesIndole SynthesisOxidative CouplingOxidative Cross-couplingRegioselectivity
The oxidative synthesis of highly functionalized indoles from simple anilines and internal alkynes mediated by a rhodium(III) catalyst is described. Good yields are obtained for a variety of aniline substrates, and good regioselectivity is obtained for the more sterically accessible position when meta -substituted anilines are used. Symmetrical and unsymmetrical alkynes react efficiently with high (>40:1) C 2/ C 3 regioselectivity when aryl/alkyl substituted alkynes are used.
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M.D.K. Boele, Gino P. F. van Strijdonck, André H. M. de Vries et al. · Journal of the American Chemical Society · 2002 · 615 citations · Full text