Publication | Closed Access
A Metal‐ and Azide‐free Oxidative Coupling Reaction for the Synthesis of [1,2,3]Triazolo[1,5‐a]quinolines and their Application to Construct C−C and C‐P Bonds, 2‐Cyclopropylquinolines and Imidazo[1,5‐a]quinolines
31
Citations
56
References
2020
Year
Broad Substrate ScopeOxidative Annulation ReactionCross-coupling ReactionDiversity Oriented SynthesisConstruct C−cNatural SciencesDiversity-oriented SynthesisIodine‐promoted One‐potC‐p BondsOrganic ChemistryOrganometallic CatalysisChemistryHeterocycle ChemistryPharmacologySynthetic Chemistry
Abstract An iodine‐promoted one‐pot cascade oxidative annulation reaction has been developed for the synthesis of [1,2,3]triazolo[1,5‐a]quinolines from methyl azaarenes and N ‐tosylhydrazines. The reaction has a broad substrate scope and can be easily scaled up to gram‐scale. 1,2,3‐Triazoles are an important skeletal structure for the construction of C−C and C−P bonds, 2‐cyclopropylquinolines and imidazo[1,5‐a]quinolines, for which different synthetic applications were explored. magnified image
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