Conclusions
The reaction of dialkylthiophosphoric and cyclic six and seven-membered thiophosphoric acids with oxetanes gives the S-3-hydroxyalkyl esters of these acids. During synthesis the S-3-hydroxyalkyl esters of the five-membered cyclic thioacids undergo rearrangement to the 3-mercaptoalkyl derivatives.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1128–1130, May, 1981.
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Nuretdinova, O.N., Arbuzov, B.A. Reaction of phosphorus monothio acids with oxetanes. Russ Chem Bull 30, 887–889 (1981). https://doi.org/10.1007/BF00955306
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DOI: https://doi.org/10.1007/BF00955306