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Regioselective acylation of methyl 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate
Authors:Yarovenko  V N  Semenov  S L  Zavarzin  I V  Ignatenko  A V  Krayushkin  M M
Institution:(1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
Abstract:The influence of catalysts, acid chlorides, and solvents on the acylation of methyl 2-methyl-4H-thieno3,2-b]pyrrole-5-carboxylate was studied. The use of AlCl3 allows the regioselective introduction of the acyl group into position 3 to be performed, whereas the acyl group is regioselectively introduced into position 6 of thienopyrrole when SnCl4 is used.
Keywords:thienopyrroles  regioselective acylation  ionic liquid
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