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Study of the possibility of forming 7- and 9-membered rings in the D-mannitol tricyclic triethyl triphosphite molecule

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

Conclusions

The transesterification reaction was used to synthesize some cyclic phosphites from the 1,3∶4,6-di- and 2,5-O-methylene-D-mannitols and 1,6-dichloro-D-mannitol. 1,4-Butylene glycol and 2,3,4,5-di-O-methylene-D-mannitol do not form cyclic phosphites under the transesterification conditions.

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Academy of Sciences of the USSR, USSR

    É. T. Mukmenev, P. A. Kirpichnikov & O. V. Voskresenskaya

  2. S. M. Kirov Kazan Chemical-Technological Institute, USSR

    É. T. Mukmenev, P. A. Kirpichnikov & O. V. Voskresenskaya

Authors
  1. É. T. Mukmenev
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  2. P. A. Kirpichnikov
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  3. O. V. Voskresenskaya
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1395–1399, June, 1972.

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Mukmenev, É.T., Kirpichnikov, P.A. & Voskresenskaya, O.V. Study of the possibility of forming 7- and 9-membered rings in the D-mannitol tricyclic triethyl triphosphite molecule. Russ Chem Bull 21, 1344–1347 (1972). https://doi.org/10.1007/BF00854559

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  • DOI: https://doi.org/10.1007/BF00854559

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