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Reaction of Substituted 2-Allylthiopyrimidin-4(3H)-ones with Sulfenyl Chlorides

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Reaction of substituted 2-allylthiopyrimidin-4(3H)-ones with p-nitrobenzosulfenyl chloride gives the products of addition at the allyl moiety, while the reaction with 2-benzothiazolyl sulfenyl chloride yields thiazolidinopyrimidines with an angular structure.

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Authors and Affiliations

  1. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, 02094

    A. I. Vaskevich, Yu. I. Gevaza, R. I. Vaskevich & V. I. Staninets

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  1. A. I. Vaskevich
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  2. Yu. I. Gevaza
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  3. R. I. Vaskevich
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  4. V. I. Staninets
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Vaskevich, A.I., Gevaza, Y.I., Vaskevich, R.I. et al. Reaction of Substituted 2-Allylthiopyrimidin-4(3H)-ones with Sulfenyl Chlorides. Chemistry of Heterocyclic Compounds 40, 1087–1091 (2004). https://doi.org/10.1023/B:COHC.0000046702.48941.53

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  • DOI: https://doi.org/10.1023/B:COHC.0000046702.48941.53

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