Publication | Closed Access
Palladium-Catalyzed Synthesis of 2-Aryl-<i>2H</i>-Benzotriazoles from Azoarenes and TMSN<sub>3</sub>
49
Citations
78
References
2015
Year
EngineeringHeterocyclicAzo NitrogenOrganic ChemistryC-n Bond FormationOrganometallic CatalysisCatalysisO-azide NitrogenChemistryPalladium-catalyzed SynthesisSynthetic ChemistryBiomolecular Engineering
Substrate-directed ortho C-H amination of azoarenes using TMSN3 as the source of nitrogen leading to the synthesis of 2-aryl-2H-benzotriazoles has been accomplished with the help of Pd/TBHP combinations. An intermolecular o-azidation (C-N bond formation) followed by an intramolecular N-N bond formation via nucleophilic attack of one of the azo nitrogen onto the o-azide nitrogen leads to cyclization with the expulsion of N2.
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