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1,3-Dipolar Cycloaddition of Ethyl Propiolate to 4,4-Dimethyl-4,5-dihydro-1,2-dithiolo-[5,4-c]quinoline-1-thiones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The interaction of ethyl propiolate with 4,4-dimethyl-4,5-dihydro-2,3-dithiolo[3,4-c]quinoline-1-thiones leads to 1,3-dithiol-2-ylidenes, 1,6,6a(l4)-trithiapentalene, or thiino[2,3-c]quinolines depending on the conditions.

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Authors and Affiliations

  1. Voronezh State University, Voronezh, 394693, Russia

    S. M. Medvedeva, Kh. S. Shikhaliev, G. I. Ermolova, A. S. Solov'ev & G. V. Shatalov

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  1. S. M. Medvedeva
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  2. Kh. S. Shikhaliev
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  3. G. I. Ermolova
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  4. A. S. Solov'ev
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  5. G. V. Shatalov
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Medvedeva, S.M., Shikhaliev, K.S., Ermolova, G.I. et al. 1,3-Dipolar Cycloaddition of Ethyl Propiolate to 4,4-Dimethyl-4,5-dihydro-1,2-dithiolo-[5,4-c]quinoline-1-thiones. Chemistry of Heterocyclic Compounds 38, 918–921 (2002). https://doi.org/10.1023/A:1020913328392

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  • DOI: https://doi.org/10.1023/A:1020913328392

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