Synthesis and structure of 2,4-dinitrophenylcyanoacetamide derivatives as CH acids and their organic salts View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2009-12

AUTHORS

Yu. G. Gololobov, I. R. Gol’ding, F. Terrie, P. V. Petrovskii, K. A. Lyssenko, I. A. Garbuzova

ABSTRACT

C-Arylation of cyanoacetamides with chloro-2,4-dinitrobenzene was performed in acetonitrile in presence of potassium carbonate. The CH acids obtained react with triethylamine or N-methylmorpholine to give salts that contain anions possessing highly conjugated system of unsaturated bonds.

PAGES

2443-2448

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-009-0342-6

DOI

http://dx.doi.org/10.1007/s11172-009-0342-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1024387265


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