Synthesis and Formylation of Substituted 2-Spiropyrimidin-4-ones and Related Compounds View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-11

AUTHORS

V. I. Markov, O. K. Farat, S. A. Varenichenko, E. V. Velikaya, R. I. Zubatyuk, O. V. Shishkin

ABSTRACT

Treatment of cyclohexanone-2-carboxamide with cyclic ketones provides oxazine derivatives while refluxing in toluene with ammonium acetate and cyclic ketones yields substituted 2-spiropyrimidin-4-ones. Depending on the ratio of reactants, the oxazines and substituted 2-spiropyrimidin-4-ones under Vilsmeier-Haack conditions undergo formylation or an electrophilic rearrangement.

PAGES

1158-1165

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-013-1358-2

DOI

http://dx.doi.org/10.1007/s10593-013-1358-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1000377588


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