α-Nitro chalcones: Structure and reaction with pyrrole View Full Text


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Article Info

DATE

2009-10

AUTHORS

V. M. Berestovitskaya, R. I. Baichurin, N. I. Aboskalova, K. A. Lysenko, G. A. Berkova, A. V. Fel’gendler

ABSTRACT

According to the 1H NMR, IR, and electronic absorption spectra and X-ray diffraction data, 2-aryl-1-benzoyl-1-nitroethenes have E configuration with predominant s-cis conformation, where the nitro group lies in the plane of the double carbon-carbon bond, while the carbonyl group deviates from that plane. Reactions of 2-aryl-1-benzoyl-1-nitroethenes with pyrrole and N-methylpyrrole gave the corresponding alkylation products at the C2 atom in the heteroring. More... »

PAGES

2191

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363209100181

DOI

http://dx.doi.org/10.1134/s1070363209100181

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1028476026


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