85059-19-4Relevant articles and documents
STRUCTURE OF CYANOETHYLATION PRODUCTS OF 1,2,3-TRIAZOLECARBOXYLIC ACID DERIVATIVES
Sedov, A. L.,Nemeryuk, M. P.,Anisimova, O. S.,Solov'eva, N. P.,Safonova, T. S.
, p. 1187 - 1191 (1994)
The cyanoethylation of derivatives of 5-chloro-1,2,3-triazolecarboxylic acids was studied, and it was shown by mass spectrometry and 1H NMR spectroscopy that the only products of this reaction are 2-N-cyanoethyl derivatives.
DERIVATIVES OF 4(5)SUBSTITUTED-1,2,3-TRIAZOL-5(4)-CARBOXYLIC ACIDS SYNTHESIS AND ANTITUMOR ACTIVITY
Nemeryuk, M. P.,Sedov, A. L.,Ryabokon, N. A.,Ershova, Yu. A.,Sokolova, A. S.,et al.
, p. 406 - 410 (2007/10/02)
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HETEROCYCLIC COMPOUNDS CONTAINING DIAZO AND CYANO GROUPS. 1. DIAZOACETONITRILE DERIVATIVES IN THE SYNTHESIS OF 5-HALO-1H-1,2,3-TRIAZOLES
Shafran, Yu. M.,Bakulev, V. A.,Mokrushin, V. S.,Alekseev, S. G.
, p. 1038 - 1043 (2007/10/02)
Carbonyl-substituted derivatives of diazoacetonitrile have been obtained by the diazotation of amines and by diazo-group transfer which, under the action of hydrogen halide, have been converted into 4-carbonyl-substitued 5-halo-1H-1,2,3-triazoles.The stru