Synthesis of 2-N-substituted benzothiazoles via domino condensation-hetero cyclization process, mediated by copper oxide nanoparticles under ligand-free conditions
A simple and highly practical method for the synthesis of 2-N-substituted benzothiazoles has been developed by using nanocopper oxide as a recyclable catalyst. The present tandem process allows to get access to a wide range of 2-N-substituted benzothiazoles in good to excellent yields by the reactio...
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Veröffentlicht in: | Tetrahedron letters 2012-05, Vol.53 (20), p.2518-2521 |
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creator | Satish, G. Reddy, K. Harsha Vardhan Ramesh, K. Karnakar, K. Nageswar, Y.V.D. |
description | A simple and highly practical method for the synthesis of 2-N-substituted benzothiazoles has been developed by using nanocopper oxide as a recyclable catalyst. The present tandem process allows to get access to a wide range of 2-N-substituted benzothiazoles in good to excellent yields by the reaction of 2-iodo aniline with carbon disulfide and piperidine in presence of KOH as a base and DMSO as a solvent under ligand-free conditions. |
doi_str_mv | 10.1016/j.tetlet.2012.03.012 |
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source | Elsevier ScienceDirect Journals Complete |
subjects | 2-N-substituted benzothiazole Carbon disulfide CATALYSTS Condensing COPPER OXIDE CuO nanoparticles FABRICATION LIGANDS MICROSTRUCTURES Nanoparticles Nanostructure OXIDES PARTICLES Piperidine Recyclability SOLVENTS Synthesis (chemistry) Tetrahedrons |
title | Synthesis of 2-N-substituted benzothiazoles via domino condensation-hetero cyclization process, mediated by copper oxide nanoparticles under ligand-free conditions |
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