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Mendeleev Communications, 2019, Volume 29, Issue 2, Pages 234–236
DOI: https://doi.org/10.1016/j.mencom.2019.03.041
(Mi mendc1483)
 

This article is cited in 7 scientific papers (total in 7 papers)

Communications

Reactions of carbamoylated amino enones with 3-substituted chromones for the preparation of 2-pyridones and chromeno[4,3-b]pyridine-2,5-diones

D. L. Obydennova, A. I. El-Tantawyab, M. Yu. Korneva, V. Ya. Sosnovskikha

a Institute of Natural Sciences and Mathematics, Ural Federal University, Ekaterinburg, Russian Federation
b Department of Physics and Engineering Mathematics, Faculty of Electronic Engineering, Menoufia University, Menouf, Egypt
Abstract: N-Aryl-5-arylamino-3-oxohex-4-enamides as 1,3-C,N-di-nucleophiles react regioselectively with 3-formyl or 3-methoxycarbonyl chromones in the presence of DMAP in MeCN to form 2-pyridones (34–43%) or chromeno[4,3-b]pyridine-2,5-diones (54–73%) bearing the amino enone moiety.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (910.9 Kb)


Citation: D. L. Obydennov, A. I. El-Tantawy, M. Yu. Kornev, V. Ya. Sosnovskikh, “Reactions of carbamoylated amino enones with 3-substituted chromones for the preparation of 2-pyridones and chromeno[4,3-b]pyridine-2,5-diones”, Mendeleev Commun., 29:2 (2019), 234–236
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  • https://www.mathnet.ru/eng/mendc1483
  • https://www.mathnet.ru/eng/mendc/v29/i2/p234
  • This publication is cited in the following 7 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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