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2-Benzothiazolylhydrazones with Cation Radicals in Nitrile Solvents. Formations of 1,2,4-Triazoles and Triazolo[3,4-b]benzothiazoles


Abstract

Arenealdehyde 2-benzothiazolylhydrazone in thianthrene cation radicalafforded triazolo[3,4-b]benzothiazoles and 1,2,4-triazoles as major and minor product, respectively. On the contrary the similar reaction in tris(2,4-dibromophenyl)aminium hexachloroantimonate gave 1,2,4-triazoles and triazolo[3,4-b]benzothiazoles as ma-jor and minor product, respectively.

Keywords

References

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Cited by

  1. An overview of some reactions of thianthrene cation radical. Products and mechanisms of their formation vol.27, pp.6, 2000, https://doi.org/10.1080/17415990600987965
  2. Arylhydrazones Derivatives Containing a Benzothiazole Moiety, Efficient Ligands in the Palladium‐Catalyzed Mizoroki–Heck and Suzuki–Miyaura Cross‐coupling Reactions under IR Ir vol.35, pp.12, 2000, https://doi.org/10.1002/cjoc.201700390