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Abnormally mild synthesis of bis(dithiolo)pyrroles from 2,5-dimethylpyrroles
Authors:Amelichev Stanislav A  Aysin Rinat R  Konstantinova Lidia S  Obruchnikova Natalia V  Rakitin Oleg A  Rees Charles W
Institution:N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect, 47, 119991 Moscow, Russia.
Abstract:chemical reaction: see text]. Treatment of N-substituted 2,5-dimethylpyrroles 2 with an equilibrated mixture of disulfur dichloride and DABCO in chloroform at 0 degrees C gives pentathiepinopyrroles 3 in moderate yields; further reaction of 3 with the same mixture at room temperature leads, in an extensive reaction cascade, to bis(dithiolo)pyrroles 4 in high yield; 2 can be converted into 4 in a one-pot operation under unusually mild conditions.
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