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Alkali-catalyzed hydration of stereoisomeric 3,4-epoxycaranes

  • É. Kh. Kazakova
  • L. N. Surkova
Brief Communications
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Conclusions

The alkali-catalyzed hydration of the stereoisomeric 3,4-epoxycaranes gives a mixture of the expected glycols, together with the skeletal rearrangement product in the case of the cis-epoxide.

Keywords

Hydration Glycol Rearrangement Product Skeletal Rearrangement 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Literature cited

  1. 1.
    É. Kh. Kazakova, L. N. Surkova, and S. V. Andreeva, Izv. Akad. Nauk SSSR, Ser. Khim., 1636 (1982).Google Scholar
  2. 2.
    H. Schmidt, P. Richter, and M. Mulstädt, Chem. Ber.,96, 2636 (1963).Google Scholar
  3. 3.
    R. R. D'yakonova, A. A. Musina, R. G. Gainullina, and A. G. Chernov, Izv. Akad. Nauk SSSR, Ser. Khim., 1327 (1982).Google Scholar
  4. 4.
    B. A. Arbuzov and Z. G. Isaeva, Usp. Khim.,8, 1339 (1976).Google Scholar

Copyright information

© Plenum Publishing Corporation 1984

Authors and Affiliations

  • É. Kh. Kazakova
    • 1
  • L. N. Surkova
    • 1
  1. 1.A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan BranchAcademy of Sciences of the USSRUSSR

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