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Reaction of triethyl phosphite withβ-substituted nitriles
Authors:B. E. Ivanov  V. F. Zheltukhin
Affiliation:(1) A. E. Arbuzov Institute of Organic and Physical Chemistry, Academy of Sciences of the USSR, USSR
Abstract:Conclusions Propionitriles having hydroxy, acetate, and phenoxy groups in thebeta-position are capable of undergoing the Arbuzov rearrangement with triethyl phosphite to form diethylbeta-cyanoethylphosphonate.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2089–2090, September, 1967.
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