Competitive formation of 4-aminoisoxazoles and 5-aminooxazoles in the cyclization reactions of O-alkylated hydroxyimino nitriles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-10

AUTHORS

V. P. Kislyi, E. B. Danilova, V. V. Semenov, A. A. Yakovenko, F. M. Dolgushin

ABSTRACT

Base-catalyzed cyclization of O-alkylated α-hydroxyimino nitriles gave mixtures of 4-aminoisoxazoles and 5-aminooxazoles, their ratio depending on the substituent structures and the reaction conditions. The formation mechanism of 5-aminooxazoles in this reaction is discussed.

PAGES

1840-1847

References to SciGraph publications

  • 1999-01. Acetyl ketene aminals in Nenitzescu reaction in RUSSIAN CHEMICAL BULLETIN
  • 2002-11. A Convenient Route to Phosphonium Derivatives of Coumarin and Its Imino Analog in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2004-12-18. Chiral cosmic strings in supergravity in JOURNAL OF HIGH ENERGY PHYSICS
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    URI

    http://scigraph.springernature.com/pub.10.1007/s11172-006-0495-5

    DOI

    http://dx.doi.org/10.1007/s11172-006-0495-5

    DIMENSIONS

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