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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
Full-text PDF (273 kB) Citations (7)
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.
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
Linking options:
  • https://www.mathnet.ru/eng/mendc1483
  • https://www.mathnet.ru/eng/mendc/v29/i2/p234
  • This publication is cited in the following 7 articles:
    1. Reena Rani, Sheetu Devi, Neelam Yadav, Sarita Sangwan, Vidhi Dhanda, Vipan Kumar, Sonu Chauhan, Anil Duhan, Ravi Kumar, “Advances in the Synthesis of 3‐Acyl‐2‐Pyridones: Strategies and Methods for Accessing the Versatile Scaffold”, Journal of Heterocyclic Chem, 2024  crossref
    2. Al-Shimaa Badran, Aya Ahmed, Magdy A. Ibrahim, “Chemical Transformation of Chromones into Coumarins”, HETEROCYCLES, 102:12 (2021), 2277  crossref
    3. Prasanta Patra, Gandhi Kumar Kar, “The synthesis, biological evaluation and fluorescence study of chromeno[4,3-b]pyridin/quinolin-one derivatives, the backbone of natural product polyneomarline C scaffolds: a brief review”, New J. Chem., 45:6 (2021), 2879  crossref
    4. Mostafa M.K. Amer, Maged A. Aziz, Wesam S. Shehab, Magda H. Abdellattif, Samar M. Mouneir, “Recent advances in chemistry and pharmacological aspects of 2-pyridone scaffolds”, Journal of Saudi Chemical Society, 25:6 (2021), 101259  crossref
    5. M. N. Elinson, Yu. E. Ryzhkova, F. V. Ryzhkov, “Multicomponent design of chromeno[2,3-b]pyridine systems”, Russian Chem. Reviews, 90:1 (2021), 94–115  mathnet  mathnet  crossref  isi  scopus
    6. M. Yu. Kornev, D. S. Tishin, D. L. Obydennov, V. Ya. Sosnovskikh, “Reactions of 3-functionalized chromones with triacetic acid lactone”, Mendeleev Commun., 30:2 (2020), 233–235  mathnet  crossref
    7. Magdy A. Ibrahim, Youssef A. Alnamer, “Ring Opening and Recyclization Reactions of 3‐Nitrochromone with Some Nucleophilic Reagents”, Journal of Heterocyclic Chem, 56:9 (2019), 2341  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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