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Alkyltriflate-Triggered Annulation of Arylisothiocyanates and Alkynes Leading to Multiply Substituted Quinolines through Domino Electrophilic Activation
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Citations
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References
2014
Year
High YieldsCross-coupling ReactionEngineeringDomino Electrophilic ActivationAlkyltriflate-triggered AnnulationTransition-metal CatalystOrganic ChemistryMultiply Substituted QuinolinesCatalysisStereoselective SynthesisChemistryHeterocycle ChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringQuinoline Ring
The reaction of arylisothiocyanate, alkyltriflate, and alkynes leads to variously substituted quinolines in high yields. The reaction undergoes alkyltriflate-triggered domino electrophilic activation and avoids the use of a transition-metal catalyst. A variety of functional groups are tolerated in the quinoline ring.
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