RECYCLIZATION OF 1,3,4-OXADIAZOLES AND BIS-1,3,4-OXADIAZOLES INTO 1,2,4-TRIAZOLE DERIVATIVES. SYNTHESIS OF 5-UNSUBSTITUTED 1,2,4-TRIAZOLES
DOI:
https://doi.org/10.1007/8244Keywords:
3, 4-diaryl-1, 2, 4-triazoles, precursors of stable carbenes, 1, 4-oxadiazoles, 3'- and 4, 4'-bridge linked bis-1, recyclization reactionAbstract
Efficient methods have been developed for obtaining precursors of stable carbenes, viz. 5-unsubstituted 3,4-diaryl-1,2,4-triazoles and 3,3'- or 4,4'-bridge linked bis-1,2,4-triazoles, by the recyclization of 5-unsubstituted 1,3,4-oxadiazoles or p-phenylenebis-1,3,4-oxadiazole with anilines or aromatic diamines in the presence of trifluoroacetic acid or with aniline hydrochlorides in pyridine.How to Cite
Korotkikh, N. I.; Kiselev, A. V.; Knishevitsky, A. V.; Raenko, G. F.; Pekhtereva, T. M.; Shvaika, O. P. Chem. Heterocycl. Compd. 2005, 41, 866. [Khim. Geterotsikl. Soedin. 2005, 1026.]
For this article in the English edition, see DOI 10.1007/s10593-005-0240-2