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Pyrroles from ketoximes and acetylene. 46. Pyrroles with sterically hindered substituents

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding pyrroles and their N-vinyl derivatives were obtained by the catalyzed (by an MOH-DMSO superbase) reaction of acetylene and its crypto forms (vinyl chloride, 1,2-dichloroethane) with alkyl-2,4-, alkyl-2,5-, and alkyl-3,4-dimethylphenylketoximes. Reaction intermediates — O-vinylketoximes — were detected.

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Literature Cited

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For Communication 45 See [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1320–1323, October, 1991.

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Aliev, I.A., Korostova, S.E., Mikhaleva, A.I. et al. Pyrroles from ketoximes and acetylene. 46. Pyrroles with sterically hindered substituents. Chem Heterocycl Compd 27, 1055–1058 (1991). https://doi.org/10.1007/BF00486796

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  • DOI: https://doi.org/10.1007/BF00486796

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