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Synthesis of Polysubstituted Cyclopentene and Cyclopenta[<i>b</i>]carbazole Analogues from Unsymmetrical 4-Arylidene-3,6-diarylhex-2-en-5-ynal and Indole Derivatives via an Iodine Mediated Electrocyclization Reaction
12
Citations
33
References
2018
Year
Iodine-promoted ElectrocyclizationDiversity Oriented SynthesisDerivativesSubstituted IndolesEngineeringIndole DerivativesNatural SciencesHeterocyclicDiversity-oriented SynthesisOrganic ChemistryPolysubstituted CyclopenteneChemistryHeterocycle ChemistryElectrocyclization ReactionsSynthetic ChemistryBiomolecular Engineering
An efficient method for the synthesis of polysubstituted cyclopentene and cyclopenta[ b]carbazole derivatives through the iodine-promoted electrocyclization of substituted indoles and 4-arylidene-3,6-diarylhex-2-en-5-ynal derivatives is reported. Polysubstituted cyclopentene derivatives were produced through 4π electrocyclization reactions with indole, 7-methylindole, and 5-bromoindole as coupling partners, whereas cyclopenta[ b]carbazole derivatives were produced via 6π electrocyclization in the case of methoxy (-OMe)-substituted indoles. The methods reported herein diastereo- and regioselectively proceed under straightforward and mild conditions.
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