Abstract
2-Aryl-4-methyl-4,5-epoxytetrahydropyrans, which react with piperidine regioselectively with trans-diaxial cleavage of the oxide ring at the least substituted carbon atom, were synthesized by the reaction of 2-aryl-4-methyl-3,6-dihydropyrans with peracids.
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A. A. Gevorkyan, A. S. Arakelyan, and N. M. Khizantsyan, Armyansk. Khim. Zh., 30, 743 (1977).
U. G. Ibatullin, D. Ya. Mukhametova, S. A. Vasil'eva, R. F. Talipov, L. V. Syurina, M. G. Safarov, and S. R. Rafikov, Izv. Akad. Nauk SSSR, Ser. Khim., No. 9, 2114 (1982).
V. B. Mochalin, Z. I. Smolina, A. I. Vul'fson, T. I. Dyumaeva, and B. V. Unkovskii, Zh. Org. Khim., No. 7, 825 (1971).
N. S. Vul'fson, G. M. Zolotareva, V. N. Bochkarev, Z. I. Smolina, B. V. Unkovskii, and V. B. Mochalin, Izv. Akad. Nauk USSR, Ser. Khim., No. 2, 437 (1970).
A. A. Gevorkyan, A. S. Arakelyan, L. I. Kazaryan, and G. G. Tokmadzhyan, Arm. Khim. Zh., 30, 685 (1977).
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Translated from Khimiya Geterotsilklicheskikh Soedinenii, No. 11, pp. 1455–1457, November, 1984.
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Ubatullin, U.G., Syurina, L.V., Vasil'eva, S.A. et al. Epoxidation of 2-aryl-4-methyl-3,6-dihydropyrans and reaction of the products with piperidine. Chem Heterocycl Compd 20, 1200–1202 (1984). https://doi.org/10.1007/BF00505705
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DOI: https://doi.org/10.1007/BF00505705