Abstract
The corresponding tetrahydrofuran derivatives were obtained by iodination of δ, ɛ- unsaturated alcohols containing substituents attached to the α-carbon atom. The effect of substituents on the stereochemistry of the products and the rate of iodination of the unsaturated alcohols were studied.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 32–34, January, 1981.
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Gevaza, Y.I., Kupchik, I.P. & Staninets, V.I. Stereochemistry of the iodocyclization of unsaturated alcohols. Chem Heterocycl Compd 17, 24–26 (1981). https://doi.org/10.1007/BF00507083
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DOI: https://doi.org/10.1007/BF00507083