Direct arylation of imidazo[2,1-b]thiazoles and thiazoles with aryl iodides via CuCl2/PPh3-catalyzed C-H bond functionalization
With PPh3 acting as a ligand, a convenient method for CuCl2‐catalyzed arylation of imidazo[1,2‐b]thiazoles and thiazoles with aryl iodides under mild reaction conditions is described. Preliminary mechanistic studies of this arylation involving a formal Cu(I) to Cu(0) and Cu(II) route by convergent d...
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Veröffentlicht in: | Applied organometallic chemistry 2015-03, Vol.29 (3), p.165-169 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | With PPh3 acting as a ligand, a convenient method for CuCl2‐catalyzed arylation of imidazo[1,2‐b]thiazoles and thiazoles with aryl iodides under mild reaction conditions is described. Preliminary mechanistic studies of this arylation involving a formal Cu(I) to Cu(0) and Cu(II) route by convergent disproportionation of the copper mediator are also reported. Copyright © 2015 John Wiley & Sons, Ltd.
A new CuCl2/PPh3‐catalyzed arylation of imidazo[1,2‐b]thiazoles and thiazoles with aryl iodides has been developed. Preliminary mechanistic studies of this arylation are also reported. This protocol provides a straightforward and operationally simple method for the synthesis of trisubstituted imidazo[1,2‐b]thiazoles and trisubstituted thiazoles. |
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ISSN: | 0268-2605 1099-0739 |
DOI: | 10.1002/aoc.3263 |