Conclusions
The N,N,N′-trifluoroamidines of unsubstituted aliphatic carboxylic acids react easily with sodium ethoxide to give the corresponding N-fluoroimino ethers and esters.
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Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2802–2803, December, 1978.
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Fokin, A.V., Stolyarov, V.P., Gukov, A.M. et al. Reaction of N,N,N′-trifluoroamidines of unsubstituted carboxylic acids with sodium ethoxide. Russ Chem Bull 27, 2502–2503 (1978). https://doi.org/10.1007/BF00941109
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DOI: https://doi.org/10.1007/BF00941109