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New derivatives of imidazoline 3-oxide and thiazoline with 2,6-dialkylphenol fragments

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

(2,6-Dialkyl-4-hydroxyphenyl)-2-butanones and aminooxides were used to obtain the corresponding 3-imidazoline 3-oxides. Nitrosylation of 3-imidazoline 3-oxide containing a phenol substituent proceeds either at the imidazoline ring amino group or at the phenol fragment. Intermolecular cyclization of (2,6-di-tert-butyl-4-hydroxyphenyl)-2-butanone with sulfur and ammonia gave a 3-thiazoline as two diastereomers.

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Authors and Affiliations

  1. Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Academy of Sciences of the USSR, 630090, Novosibirsk

    T. F. Titova, A. P. Krysin & V. V. Martin

Authors
  1. T. F. Titova
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  2. A. P. Krysin
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  3. V. V. Martin
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 62–67, January, 1986.

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Titova, T.F., Krysin, A.P. & Martin, V.V. New derivatives of imidazoline 3-oxide and thiazoline with 2,6-dialkylphenol fragments. Chem Heterocycl Compd 22, 52–56 (1986). https://doi.org/10.1007/BF00515423

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  • DOI: https://doi.org/10.1007/BF00515423

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