Chemical Communications · 2022 · 16 citations · 27 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryAddition ReactionsCross-coupling ReactionsHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic SynthesisElectrophilic Aromatic SubstitutionElectrophilic Substitution In HeterocyclesIsoquinoline SynthesisMild Reaction ConditionsQuinoline SynthesisScopeTriazole Chemistry
azaarene, at their α-position. Subsequent ylide formation and intramolecular 1,5-cyclization furnished 4,3-fused 1,2,4-triazolyl-azaarenes in good yields. The reaction is notable for its mild conditions, operational simplicity and fairly general scope.
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How Nucleophilic Are Diazo Compounds?
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