Conclusions
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1.
The silylation of the Ag salt of N-nitro-p-toluenesulfonamide with trimethylchlorosilane, or of the free N-nitro-p-toluenesulfonamide with N,N′-diphenyl-N-trimethylurea, gave the O-trimethylsilyl derivative of N-nitro-p-toluenesulfonamide.
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2.
The reaction of the Ag salt of N-nitro-p-toluenesulfonamide with diethylboron chloride gave the O-diethylboron derivative of N-nitro-p-toluenesulfonamide. Treatment of the derivative with pyridine gave the bis(pyridyldiethylboronium) salt of N-nitro-p-toluenesulfonamide.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1146–1151, May, 1975.
The authors express their gratitude to O. A. Luk'yanov and N. I. Shlykova for supplying the samples of compounds (IV) and (V), and for the information on the IR spectra of these products.
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Ioffe, S.L., Leont'eva, L.M., Makarenkova, L.M. et al. Synthesis and structure of trimethylsilyl and diethylboron derivatives of p-toluene-N-nitrosulfonamide. Russ Chem Bull 24, 1053–1056 (1975). https://doi.org/10.1007/BF00922963
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DOI: https://doi.org/10.1007/BF00922963