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A set of electrophilic 2-(trifluoroacetyl)-1,3-azoles demonstrated- excellent activity in the C-oxyalkylation of pyrrole, furan, thiophene, 1,3-thiazole, and 1,2-oxazole derivatives. The reaction conditions and the yields of the corresponding trifluoromethyl-substituted alcohols depend strongly on both the electronic and steric nature of the 1,3-azole unit. Georg Thieme Verlag Stuttgart ? New York.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 1603-91-4. In my other articles, you can also check out more blogs about 1603-91-4
Reference：
Thiazole | C3H9880NS – PubChem,
Thiazole | chemical compound | Britannica