Regioselective acylation of methyl 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate |
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Authors: | Yarovenko V N Semenov S L Zavarzin I V Ignatenko A V Krayushkin M M |
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Institution: | (1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation |
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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. |
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Keywords: | thienopyrroles regioselective acylation ionic liquid |
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