Conclusions
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1.
A series of 4-aryl-1, 2-dithiole-3-thiones and 4-aryl-1, 2-dithiolium salts, as well as two 5-aryl-1,2-dithiole-3-thiones, have been synthesized, and their choleretic activities have been investigated.
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2.
The 5-aryl-1,2-dithiole-3-thione is more active in its choleretic effect than is the 4-isomer. The 4-aryl-1,2-dithiolium derivatives are more effective than the corresponding 4-aryl-1,2-dithiole-3-thiones. The choleretic activity of the 5-(p-methoxyphenyl)-1, 2-dithiole-3-thione that was synthesized did not seem to be as high as has been claimed in the literature.
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Translated from Khimiko-Farmatsevticheskii Zhurnal, No. 11, pp. 18–23, November, 1967.
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Voronkov, M.G., Lanina, T.V., Saratikov, A.S. et al. Synthesis of several 4-aryl derivatives of 1,2-dithiole-3-thione and 1, 2-ditholium and their choleretic activity. Pharm Chem J 1, 621–625 (1967). https://doi.org/10.1007/BF00760820
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DOI: https://doi.org/10.1007/BF00760820