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Reaction of (−)-carvone with phenylmethanethiol in the presence of basic Csβ-zeolite

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Abstract

Reaction of (−)-carvone with phenylmethanethiol in the presence of basic Csβ-zeolite gave products of hetero-Michael addition. Two stereoisomeric products of addition of phenylmethanethiol at the endocyclic double carbon-carbon bond of (−)-carvone were isolated and characterized.

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Authors and Affiliations

  1. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, pr. Akademika Lavrent’eva 9, Novosibirsk, 630090, Russia

    E. V. Suslov, K. P. Volcho, D. V. Korchagina & N. F. Salakhutdinov

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  1. E. V. Suslov
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  2. K. P. Volcho
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  3. D. V. Korchagina
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  4. N. F. Salakhutdinov
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Correspondence to E. V. Suslov.

Additional information

Original Russian Text © E.V. Suslov, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov, 2010, published in Zhurnal Organicheskoi Khimii, 2010, Vol. 46, No. 4, pp. 514–516.

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Suslov, E.V., Volcho, K.P., Korchagina, D.V. et al. Reaction of (−)-carvone with phenylmethanethiol in the presence of basic Csβ-zeolite. Russ J Org Chem 46, 503–505 (2010). https://doi.org/10.1134/S1070428010040093

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  • DOI: https://doi.org/10.1134/S1070428010040093

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