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Cyclic acetals from 3,6-di-tert-butylpyrocatechol

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

The hydroxyl groups in 3,6-di-tert-butylpyrocatechol were protected by converting it to either cyclic acetals or ketals.

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Literature cited

  1. W. Baker, J. Chem. Soc., 1678 (1934).

  2. L. Taimr, H. Pivkova, and J. Pospisil, Tetrahedron Lett., 3707 (1968).

  3. H. Haeussler and W. D. Arndt, German Patent No. 1,084,260, June 30,1960 (Cl. 120); Chem. Abstr.55, 18667f (1961).

    Google Scholar 

  4. G. Sloff, Proc. Acad. Sci. Amsterdam,35, 1250 (1932).

    Google Scholar 

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2808–2810, December, 1973.

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Belostotskaya, I.S., Dzhuaryan, É.V. & Ershov, V.V. Cyclic acetals from 3,6-di-tert-butylpyrocatechol. Russ Chem Bull 22, 2744–2745 (1973). https://doi.org/10.1007/BF00926157

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  • DOI: https://doi.org/10.1007/BF00926157

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