Publication | Closed Access
Solid-Phase Synthesis of Indolecarboxylates Using Palladium-Catalyzed Reactions
96
Citations
38
References
2003
Year
Immobilized EnaminoestersCross-coupling ReactionSolid-phase SynthesisEngineeringNatural SciencesPalladium-catalyzed Cyclization ReactionsDiversity-oriented SynthesisCatalytic SynthesisOrganic ChemistryTandem Heck-amination ReactionsCatalysisChemistrySynthesis MethodSynthetic ChemistryBiomolecular Engineering
Polymer-supported, palladium-catalyzed cyclization reactions effectively synthesized indolecarboxylates. Palladium-catalyzed carbon-carbon bond-forming reactions of immobilized enaminoesters followed by transesterification yielded indole 2- or 3-carboxylates with various functional groups on the benzene ring. Indolecarboxylates were efficiently cyclized via an intramolecular palladium-catalyzed amination reaction of immobilized N-substituted dehydrohalophenylalanines, and immobilized N-acetyl-dehydroalanines were efficiently converted into indolecarboxylates via tandem Heck-amination reactions.
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