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Iodocyclization of 2-allylcyclohexanols

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Iodination of 2-allylcyclohexanol and its 1-methyl and 1-phenyl derivatives gives the corresponding 2-(iodomethyl)octahydrobenzofurans. These are reduced by to the stereoisomeric 2-methyloctahydrobenzofurans. The rate of iodination of 2-allylcyclohexanols is largely independent of their configuration.

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Literature cited

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Authors and Affiliations

  1. Institute of Organic Chemistry, Academy of Sciences of the Ukrainian SSR, 252660, Kiev

    Yu. I. Gevaza, I. P. Kupchik, V. I. Staninets, V. N. Kalinin & A. G. Bratolyubova

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  1. Yu. I. Gevaza
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  2. I. P. Kupchik
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  3. V. I. Staninets
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  4. V. N. Kalinin
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  5. A. G. Bratolyubova
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 170–172, February, 1985.

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Gevaza, Y.I., Kupchik, I.P., Staninets, V.I. et al. Iodocyclization of 2-allylcyclohexanols. Chem Heterocycl Compd 21, 135–137 (1985). https://doi.org/10.1007/BF00504193

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  • DOI: https://doi.org/10.1007/BF00504193

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