Publication | Closed Access
Synthesis of Nitroalkenes Involving a Cooperative Catalytic Action of Iron(III) and Piperidine: A One‐Pot Synthetic Strategy to 3‐Alkylindoles, 2<i>H</i>‐Chromenes and <i>N</i>‐Arylpyrrole
54
Citations
55
References
2013
Year
Chemical EngineeringCross-coupling ReactionEngineeringOne‐pot Synthetic StrategyNatural SciencesDiversity-oriented SynthesisCooperative Catalytic ActionCooperative Catalytic ReactionOrganic ChemistryCooperative Catalytic SystemOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryCatalytic SynthesisSimple Strategy
Abstract An efficient and simple strategy has been developed to synthesize various substituted nitroalkenes involving a cooperative catalytic system of FeCl 3 and piperidine. This dual catalytic protocol simultaneously activates both electrophile and nucleophile and works under mild reaction conditions so that many sensitive functional groups were tolerated. Moreover, this cooperative catalytic reaction is also suitable for various one‐pot reactions involving nitroalkenes such as, 2 H ‐chromenes, N ‐arylpyrrole and Michael reaction with indole. Notably, this method is low‐cost, efficient and environmentally friendly.
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