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New 4(5H)-oxazolonium perchlorate derivatives

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The condensation of 2,3-dimethyl-4(5H)-oxazolonium salts with ethyl orthoformate and amides of 5-substituted 2-furancarboxylic acids gives the corresponding products derived by modification of the methyl group at C(2), 2-formylmethylene-4-oxazolidinone and 2-furoylaminoethenyl-4(5H)-oxazolanium perchlorates.

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References

  1. V. G. Kul'nevich, T. P. Kosulina, F. U. Lyubke, and Z. I. Zelikman, Khim. Geterotsikl. Soedin., No. 1, 30 (1980).

  2. F. U. Lyubke, T. P. Kosulina, and V. G. Kul'nevich, Khim. Geterotsikl. Soedin., No. 7, 894 (1981).

  3. V. V. Mezheritskii, E. P. Olekhnovich, S. M. Luk'yanov, and G. N. Dorofeenko, Orthoesters in Organic Synthesis [in Russian], Izd. Rostovsk. Univ., Rostov-on-the-Don (1976), p. 161.

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Additional information

Kuban State Technological University, 350072, Krasnodar. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 236–237, February, 1995. Original article submitted September 30, 1994.

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Kosulina, T.P., Kozlovskaya, I.N., Bychenko, N.V. et al. New 4(5H)-oxazolonium perchlorate derivatives. Chem Heterocycl Compd 31, 206–207 (1995). https://doi.org/10.1007/BF01169681

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  • DOI: https://doi.org/10.1007/BF01169681

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