Abstract
A method is proposed for replacing the nitro group in 4-nitro-3-chlorofuroxan using trimethylsityl derivatives of secondary amines and amidoximes.
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R. Calvino, A. Gasco, and A. Serafino, J. Chem. Soc. Perkin Trans. 11, 1240 (1981).
A. Gasco, V. Mortarini, Y. Rua, and A. Serafino, J. Heterocycl. Chem.,10, 587 (1973).
T. I. Godovikova, O. A. Rakitin, S. P. Golova, S. A. Vozchikova, and L. I. Khmel'nitskii, Mendeleev Commun., 209 (1993).
H. Wieland, Ber.,42, 4192 (1901).
O. A. Rakitin, T. I. Godovikova, Yu. A. Strelenko, and L. I. Khmel'nitskii, Izv. Akad. Nauk., Ser. Khim., 2398 (1986).
J. F. Klebe, in: Advances in Chemistry, E. C. Taylor (ed.), Vol. 8 (1972), p. 101.
O. A. Rakitin, V. A. Ogurtsov, Yu. A. Strelenko, and L. I. Khmel'nitskii, Izv. Akad. Nauk., Ser. Khim., 1020 (1990).
A. B. Goel and V. D. Gupta, J. Organometal. Chem.,72, 171 (1974).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1133–1135, August, 1994.
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Zavarzina, O.V., Rakitin, O.A. & Khmel'nitskii, L.I. Nitro group substitution in nitrochlorofuroxan using N- and O-triiviethylsilyl derivatives. Chem Heterocycl Compd 30, 979–981 (1994). https://doi.org/10.1007/BF01165040
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DOI: https://doi.org/10.1007/BF01165040