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Reaction of 2,4,6-triisopropyl-1,3,5-dioxaphosphorinane and its sulfide with chloral and p-fluorobenzaldehyde

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

Conclusions

In contrast to aliphatic aldehydes, the reaction of 2,4,6-triisopropyl-1,3,5-dioxaphosphorinane and its sulfide with chloral and p-fluorobenzaldehyde, does not stop at the addition stage, but proceeds, with oxidation, to the formation of oxides.

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Authors and Affiliations

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

    B. A. Arbuzov, O. A. Erastov, S. N. Ignat'eva, T. A. Zyablikova & I. P. Romanova

Authors
  1. B. A. Arbuzov
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  2. O. A. Erastov
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  3. S. N. Ignat'eva
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  4. T. A. Zyablikova
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  5. I. P. Romanova
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2776–2780, December, 1981.

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Arbuzov, B.A., Erastov, O.A., Ignat'eva, S.N. et al. Reaction of 2,4,6-triisopropyl-1,3,5-dioxaphosphorinane and its sulfide with chloral and p-fluorobenzaldehyde. Russ Chem Bull 30, 2312–2316 (1981). https://doi.org/10.1007/BF00963696

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  • DOI: https://doi.org/10.1007/BF00963696

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