Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5212237 | Tetrahedron | 2017 | 12 Pages |
Abstract
An environment benign process has been developed for the regioselective synthesis of 5-iodo-1,4-disubstituted-1,2,3-triazoles catalyzed by CuI/β-CD in water. Moreover, the process was manifested for the efficient synthesis of 2-iodo-imidazo[1,2-a]pyridines and 2-iodo-benzoimidazo[2,1-b]thiazoles in aqueous medium. Additionally, the iodinated derivatives were successfully modified via palladium catalyzed coupling reactions. The salient features of this methodology are in-situ formation of 1-iodoalkyne & alkyl/aryl azide under mild reaction conditions, high regio-selectivity and use of water as a greener solvent.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Divya Dheer, Ravindra K. Rawal, Virender Singh, P.L. Sangwan, Parthasarathi Das, Ravi Shankar,