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Behavior of acetates of furanosyl fluorides under protolysis conditions in gaseous phase

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

Conclusions

The behavior of acetates of glycofuranosyl fluorides under protolysis conditions in the gaseous phase is mainly determined by the relative configurations of the substituents at C1 and C4 atoms: the cis isomers form the [MH-HF]+ ions with higher probability, and the trans isomers, the [MH-AcOH]+ ions.

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Literature cited

  1. V. I. Kadentsev, I. A. Trushkina, O. S. Chizhov, and Ya. V. Voznyi, Izv. Akad. Nauk SSSR, Ser. Khim., 2580 (1987).

  2. Ya. V. Voznyi, I. S. Kalicheva, and A. A. Galoyan, Bioorg. Khim.,7, 406 (1981).

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  3. A. A. Solov'ev, V. I. Kadentsev, and O. S. Chizhov, Izv. Akad. Nauk SSSR, Ser. Khim., 2256 (1976).

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow

    V. I. Kadentsev, I. A. Trushkina, O. S. Chizhov & Ya. V. Voznyi

  2. Institute of Biochemistry, Academy of Sciences of the Armenian SSR, Erevan

    V. I. Kadentsev, I. A. Trushkina, O. S. Chizhov & Ya. V. Voznyi

Authors
  1. V. I. Kadentsev
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  2. I. A. Trushkina
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  3. O. S. Chizhov
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  4. Ya. V. Voznyi
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2708–2711, December, 1987.

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Kadentsev, V.I., Trushkina, I.A., Chizhov, O.S. et al. Behavior of acetates of furanosyl fluorides under protolysis conditions in gaseous phase. Russ Chem Bull 36, 2510–2512 (1987). https://doi.org/10.1007/BF00957222

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  • DOI: https://doi.org/10.1007/BF00957222

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