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Reactions of Epoxides Prepared from Some Monoterpenes with Acetic Anhydride on Aluminosilicate Catalysts

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Abstract

Reactions of epoxides prepared from α-, β-pinenes and camphene with acetic anhydride on aluminosilicate catalysts (clay K-10, zeolite β) were investigated affording various products of skeleton rearrangements: mono- and diacetates with five- and six-membered rings, and also with norbornane and pinane cores.

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Authors and Affiliations

  1. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk, 630090, Russia

    L. E. Tatarova, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov & V. A. Barkhash

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  1. L. E. Tatarova
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  2. D. V. Korchagina
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  3. K. P. Volcho
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  4. N. F. Salakhutdinov
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  5. V. A. Barkhash
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Tatarova, L.E., Korchagina, D.V., Volcho, K.P. et al. Reactions of Epoxides Prepared from Some Monoterpenes with Acetic Anhydride on Aluminosilicate Catalysts. Russian Journal of Organic Chemistry 39, 1076–1082 (2003). https://doi.org/10.1023/B:RUJO.0000010173.38389.06

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  • DOI: https://doi.org/10.1023/B:RUJO.0000010173.38389.06

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