Abstract
4-Methyl-5-phenoxy-5,6-dihydropyrans were synthesized by the reaction of 3,4-dibromo-4-methyltetrahydropyran with a number of substituted phenols. The products are converted to the corresponding phenols under the conditions of the Claisen rearrangement.
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A. A. Gevorkyan, P. I. Kazarin, N. N. Khizantsyan, A. S. Arakelyan, and G. A. Panosyan, Khim. Geterotsikl. Soedin., No. 8, 1025 (1981).
L. A. Kazitsina and I. B. Kupletskaya, Application of UV, IR, NMR, and Mass Spectroscopy in Organic Chemisltry, tin Russian], Izd. MGU, (1979), p. 68.
Organic Reactions [Russian translation], Collective Vol. 2, Inostr. Lit. (1950), p. 7.
H. Schmid, Gazz. Chim. Ital., 92, 968 (1962).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 315–317, March, 1985.
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Ibatullin, U.G., Sagitdinova, K.F., Talipova, G.R. et al. Synthesis and rearrangement of phenyl ethers of 5,6-dihydropyrans. Chem Heterocycl Compd 21, 259–262 (1985). https://doi.org/10.1007/BF00506659
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DOI: https://doi.org/10.1007/BF00506659