Chemical Modification of Plant Alkaloids. 7. T-Reaction of an Aloperine Derivative View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-07

AUTHORS

K. A. Krasnov, V. G. Kartsev, E. V. Dobrokhotova, E. K. Kultyshkina, T. V. Timofeeva, V. N. Khrustalev

ABSTRACT

N-(2-Carboxy-5-nitrophenyl)aloperine was prepared from aloperine and 2-fluoro-5-nitrobenzaldehyde and condensed with 1,3-dimethylbarbituric acid via a T-reaction with opening of the piperidine ring and formation of 1,3-dimethyl-5-{5-nitro-2-[3-(10-oxo-7-azatricyclo[7.3.1.02,7]trideca-11-en-12-yl)propylamino]} benzylhexahydro-2,4,6-pyrimidinetrione. The structure of the prepared compound was studied by an X-ray crystal structure analysis.

PAGES

703-707

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10600-017-2095-z

DOI

http://dx.doi.org/10.1007/s10600-017-2095-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1090754400


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147 rdf:type schema:Organization
 




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