Conclusions
The tendency toward cyclization with the loss of phenol or dialkylamine and formation of compounds with a 1, 3, 3-thiaoxaphosphorinane ring decreases in the series of 3-hydroxyalkyl esters of diphenythiophosphoric, alkyl-O-phenylthiophosphonic, phenyl-O-phenylthiophosphonic, and alkyldialkylamidothiophosphonic acids.
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Literature cited
O. N. Nuretdinova and B. A. Arbuzov, Izv. Akad. Nauk SSSR, Ser. Khim., 1130 (1981).
B. A. Arbuzov and O. N. Nuretdinova, Izv. Akad. Nauk SSSR, Ser. Khim., 675 (1983).
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1197–1200, May, 1985.
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Nuretdinova, O.N., Novikova, V.G. Transformations of hydroxyalkyl esters of thiophosphonic acids containing a phenoxy or dialkylamido group at the phosphorus atom. Russ Chem Bull 34, 1096–1098 (1985). https://doi.org/10.1007/BF01142812
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DOI: https://doi.org/10.1007/BF01142812