Publication | Closed Access
Transition‐Metal‐Mediated Routes to 3,3‐Disubstituted Oxindoles through Anilide Cyclisation
308
Citations
127
References
2011
Year
Chemical EngineeringCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisAnilide CyclisationOrganic ChemistryOrganometallic CatalysisCatalysisChemistryBond FormationSynthesis MethodNatural Product SynthesisHeck Reaction
Abstract This review describes transition‐metal‐catalysed and ‐mediated processes for the preparation of oxindoles from anilides through C(3)–C(3a) bond formation. Traditional methods, such as the Heck reaction, and recent developments, including direct Ar–H coupling processes, are presented, as are applications in natural product synthesis.
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