Diphenylmethyl and tetrahydropyranyl protecting groups in the synthesis of 3-substituted 5-amino- and 5-hydrazino-1,2,4-triazoles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2007-12

AUTHORS

V. V. Tolstyakov, I. V. Tselinskii, N. A. Dreving

ABSTRACT

The use of hydrazine as reagent in nucleophilic substitution and reduction in the 1,2,4-triazole series in combination with introduction of labile protecting groups makes it possible to synthesize 5-hydrazino-3-nitro-1H-1,2,4-triazole and 3-chloro-5-hydrazino-1H-1,2,4-triazol-5-ylhydrazine which were difficultly accessible previously, as well as to extend the series of 3-substituted 5-amino-1H-1,2,4-triazoles.

PAGES

2179-2185

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s107036320712016x

DOI

http://dx.doi.org/10.1134/s107036320712016x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1025556427


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