Abstract
Pyrrole-2-dithiocarboxylates were obtained by reacting alkylpyrroles with carbon disulfide in the presence of alkyl halides in the KOH-DMSO system. The pyrrole and its aryl derivatives were primarily converted into pyrrole-1-dithiocarboxylates in these conditions. The electronic structure and redox properties of the synthesized compounds were investigated by polarography and cyclic voltammetry.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii. No. 1, pp. 47–54, January, 1995.
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Sobenina, L.N., Protasova, L.E., Sergeeva, M.P. et al. Synthesis and redox properties of pyrroledithiocarboxylic acid esters. Chem Heterocycl Compd 31, 40–46 (1995). https://doi.org/10.1007/BF01171288
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DOI: https://doi.org/10.1007/BF01171288