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Mendeleev Communications, 2015, Volume 25, Issue 4, Pages 310–311
DOI: https://doi.org/10.1016/j.mencom.2015.07.028
(Mi mendc2392)
 

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

Communications

Unusual reactions of 6-amino-1,3-dimethyluracil with some aliphatic aldehydes

Yu. A. Azeva, O. S. Ermakovaa, A. M. Gibora, M. A. Ezhikovab, M. I. Kodessb, V. S. Bersenevaa

a Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation
b I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Full-text PDF (365 kB) Citations (7)
Abstract: 6-Amino-1,3-dimethyluracil reacts with two molecules of alkanals (butanal or pentanal) in formic acid to give 1,3,7,9-tetramethyl- 2,4,6,8-tetraoxopyrido[2,3-d][6,5-d’]dipyrimidine and the corresponding 3,4-dialkyl-substituted 6,8-dimethyl-5,7-dioxopyrido[2,3-d]- pyrimidines.
Document Type: Article
Language: English


Citation: Yu. A. Azev, O. S. Ermakova, A. M. Gibor, M. A. Ezhikova, M. I. Kodess, V. S. Berseneva, “Unusual reactions of 6-amino-1,3-dimethyluracil with some aliphatic aldehydes”, Mendeleev Commun., 25:4 (2015), 310–311
Linking options:
  • https://www.mathnet.ru/eng/mendc2392
  • https://www.mathnet.ru/eng/mendc/v25/i4/p310
  • This publication is cited in the following 7 articles:
    1. Mohamed M. Hammouda, Khaled M. Elattar, Ayman Y. El-Khateeb, Sahar E. Hamed, Amany M. A. Osman, “Developments of pyridodipyrimidine heterocycles and their biological activities”, Mol Divers, 28:2 (2024), 927  crossref
    2. Zeinab Hussain, Magdy A. Ibrahim, Nasser M. El-Gohary, Yassin A. Gabr, Hassan A. Allimony, Al-Shimaa Badran, “Utility of 6-Aminouracils for Building Substituted and Heteroannulated Pyrimidines: A Comprehensive Review”, HETEROCYCLES, 106:4 (2023), 594  crossref
    3. Arvind Singh, Bhupinder Kaur, Aditi Sharma, Anu Priya, Manmeet Kaur, Mussarat Shamim, Bubun Banerjee, “One-pot multi-component synthesis of diverse bioactive heterocyclic scaffolds involving 6-aminouracil or its N-methyl derivatives as a versatile reagent”, Physical Sciences Reviews, 8:10 (2023), 3475  crossref
    4. Zeinab Hussain, Magdy A. Ibrahim, Nasser M. El-Gohary, Al-Shimaa Badran, “Synthesis, characterization, DFT, QSAR, antimicrobial, and antitumor studies of some novel pyridopyrimidines”, Journal of Molecular Structure, 1269 (2022), 133870  crossref
    5. Nibedita Baruah Dutta, Jugal Bori, Pinku Gogoi, Gakul Baishya, “Metal‐, Photocatalyst‐, Light‐ and Electrochemical‐Free C‐3 Trifluoromethylation of Quinoxalin‐2(1H)‐ones, Imidazo[1,2‐a]pyridines and 2H‐Indazoles”, ChemistrySelect, 6:7 (2021), 1471  crossref
    6. Yurii A. Azev, Ol'ga S. Ermakova, Alexey M. Gibor, Marina A. Ezhikova, Mikhail I. Kodess, Vera S. Berseneva, “ChemInform Abstract: Unusual Reactions of 6‐Amino‐1,3‐dimethyluracil with Some Aliphatic Aldehydes.”, ChemInform, 47:1 (2016)  crossref
    7. Yu. A. Azev, O. S. Ermakova, A. M. Gibor, V. A. Bakulev, M. A. Ezhikova, M. I. Kodess, “Synthesis of pyrido[2,3-d]pyrimidines from 6-amino-1,3-dimethyluracil and aldehydes”, Russ J Org Chem, 51:12 (2015), 1784  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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