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First example of the coupling of α-diazoketones with thiourea: a novel route for the synthesis of 2-aminothiazoles
✍ Scribed by J.S. Yadav; B.V. Subba Reddy; Y. Gopala Rao; A.V. Narsaiah
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 131 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
a-Diazoketones undergo smooth coupling with thiourea in the presence of 10 mol % of copper(II) triflate to produce the corresponding 2-aminothiazoles in excellent yields with high selectivity. The use of copper(II) triflate makes this method simple, convenient and practical. This method works well with both aryl and alkyl diazoketones to furnish a wide range of 2-aminothiazoles.
📜 SIMILAR VOLUMES
Glycals undergo smooth carbon-Ferrier rearrangement with isocyanides in the presence of a catalytic amount of FeCl 3 under mild reaction conditions to provide C-glycosyl amides in good yields with high a-selectivity. The use of FeCl 3 makes this method simple, convenient and cost-effective. This is