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Heterocyclization of Allyloxyiodination Products of Halogen-Substituted Styrenes

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Abstract

A procedure has been proposed for the synthesis of 2-aryl-5-methyl-1,4-dioxanes by alkoxyiodination of halogen-substituted styrenes with allyl alcohol in the presence of crystalline iodine, (NaK)4CaAl6Si30O72 clinoptilolite, and silicotungstic acid sodium salt Na4SiW12O40·19H2O in aqueous medium.

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Authors and Affiliations

  1. Azerbaijan Technical University, 1073, Baku, Azerbaijan

    G. M. Talybov

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  1. G. M. Talybov
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Correspondence to G. M. Talybov.

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Translated from Zhurnal Organicheskoi Khimii, 2021, Vol. 57, No. 6, pp. 891–894 https://doi.org/10.31857/S0514749221060136.

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Talybov, G.M. Heterocyclization of Allyloxyiodination Products of Halogen-Substituted Styrenes. Russ J Org Chem 57, 1009–1011 (2021). https://doi.org/10.1134/S1070428021060191

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  • DOI: https://doi.org/10.1134/S1070428021060191

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