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Mendeleev Communications, 2012, Volume 22, Issue 2, Pages 85–86
DOI: https://doi.org/10.1016/j.mencom.2012.03.011
(Mi mendc2748)
 

This article is cited in 4 scientific papers (total in 4 papers)

Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles

V. P. Kislyi, E. B. Danilova, V. V. Semenov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Treatment of 5-benzoyl-4-(iodoacetylamino)isoxazoles with alcoholic ammonia leads to isoxazolo[4,5-e][1,4]diazepin-5-ones, whereas the analogous chloroacetylamino derivatives are converted into a mixture of the deacylated 4-aminoisoxazoles and isoxazolo- [4,5-d]pyrimidines.
Keywords: isoxazolo[4,5-e][1,4]diazepin-5-one, 4-aminoisoxazole, basicity.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (224.3 Kb)


Citation: V. P. Kislyi, E. B. Danilova, V. V. Semenov, “Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles”, Mendeleev Commun., 22:2 (2012), 85–86
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  • https://www.mathnet.ru/eng/mendc/v22/i2/p85
  • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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