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Catalytic Tetrazole Synthesis via [3+2] Cycloaddition of NaN<sub>3</sub> to Organonitriles Promoted by Co(II)-complex: Isolation and Characterization of a Co(II)-diazido Intermediate

Archana Babu, Arup Sinha

2024ACS Omega25 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide The [3+2] cycloaddition of sodium azide to nitriles to give 5-substituted 1H-tetrazoles is efficiently catalyzed by a Cobalt(II) complex ( 1 ) with a tetradentate ligand N, N -bis(pyridin-2-ylmethyl)quinolin-8-amine. Detailed mechanistic investigation shows the intermediacy of the cobalt(II) diazido complex ( 2 ), which has been isolated and structurally characterized. Complex 2 also shows good catalytic activity for the synthesis of 5-substituted 1H-tetrazoles. These are the first examples of cobalt complexes used for the [3+2] cycloaddition reaction for the synthesis of 1H-tetrazoles under homogeneous conditions.

Topics & Concepts

CycloadditionSodium azideTetrazoleCatalysisCobaltChemistryAzideIsolation (microbiology)Combinatorial chemistryMedicinal chemistryOrganic chemistryBioinformaticsBiologySynthesis of Tetrazole Derivatives