Cyclocondensation of 3(5)-Aminopyrazoles with Arylglyoxals and Cyclohexane-1,3-diones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-10

AUTHORS

O. N. Petrova, L. L. Zamigailo, M. G. Shirobokova, S. V. Shishkina, O. V. Shishkin, V. I. Musatov, V. V. Lipson

ABSTRACT

Partly hydrogenated 4-aroyl-substituted pyrazolo[3,4-b]quinolin-5-ones and 5-aroyl-substituted pyrazolo[1,5-a]quinazolin-6-ones were obtained by three-component cyclocondensation of substituted 3(5)-aminopyrazoles with the arylglyoxal hydrates and dimedone, 1,3-cyclohexanedione, or 4,4-dimethylcyclohexanedione in an alcohol medium. The chemical transformations of pyrazolo[3,4-b]quinolin5-ones in reactions with hydrazine hydrate and also upon alkylation, acylation, and oxidation were studied.

PAGES

955-967

References to SciGraph publications

  • 2010-07-27. Microwave Irradiation and Multicomponent Reactions in SYNTHESIS OF HETEROCYCLES VIA MULTICOMPONENT REACTIONS II
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-013-1332-z

    DOI

    http://dx.doi.org/10.1007/s10593-013-1332-z

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