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Cyclization of α-terpenols and their acetates by fluorosulfonic acid

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Abstract

It has been shown that the superacid cyclization of α-terpenols and their acetates takes place with structural selectivity and chemo- and stereospecificity and leads to cyclic isoprenoids with higher yields than the cyclization of the corresponding β-terpenols and their acetates.

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Authors
  1. N. D. Ungur
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  2. N. P. Popa
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  3. Nguen Van Tuen
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  4. P. F. Vlad
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Additional information

Institute of Chemistry, Academy of Sciences of the Republic of Moldova, Kishinev. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 542–548, July–August, 1993.

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Ungur, N.D., Popa, N.P., Van Tuen, N. et al. Cyclization of α-terpenols and their acetates by fluorosulfonic acid. Chem Nat Compd 29, 473–478 (1993). https://doi.org/10.1007/BF00630573

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  • DOI: https://doi.org/10.1007/BF00630573

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