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The reactions of arylazasydnones with S- and O-nucleophiles

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Chemistry of Heterocyclic Compounds Aims and scope

A series of 3-arylazasydnone derivatives containing a chlorine atom and nitro group at various phenyl ring locations were functionalized by a method developed on the basis of reactions with different S- and O-nucleophiles. In all cases, an SNAr reaction was shown to occur where the leaving group could be either a halogen or azasydnone moiety, depending on their mutual position.

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow, 119991, Russia

    Alexandr V. Kormanov, Tatyana K. Shkineva & Igor L. Dalinger

Authors
  1. Alexandr V. Kormanov
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  2. Tatyana K. Shkineva
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  3. Igor L. Dalinger
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Correspondence to Igor L. Dalinger.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2023, 59(4/5), 289–298

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Kormanov, A.V., Shkineva, T.K. & Dalinger, I.L. The reactions of arylazasydnones with S- and O-nucleophiles. Chem Heterocycl Comp 59, 289–298 (2023). https://doi.org/10.1007/s10593-023-03195-x

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