Rearrangements of 1-oxa-2-azoles. 4. Synthesis and rearrangement of isoxazole- and 4,5-dihydroisoxazole-3-carboxylic acid amidoximes View Full Text


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Article Info

DATE

1991-06

AUTHORS

V. G. Andrianov, V. G. Semenikhina, A. V. Eremeev

ABSTRACT

Isoxazole- and 4,5-dihydroisoxazole-3-carboxylic acid amidoximes were obtained in the reaction of 5-trifluoromethyl-1,2,4-oxadiazole-3-carbohydroximic acid bromide in the presence of sodium bicarbonate with monosubstituted ethylenes and acetylenes with subsequent opening of the oxadiazole ring. Amidoximes of the isoxazole series undergo rearrangement to aminofurazans under the influence of alkalis.

PAGES

651-656

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00472518

DOI

http://dx.doi.org/10.1007/bf00472518

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037951204


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