Mendeleev Communications
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Mendeleev Commun.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Mendeleev Communications, 2014, Volume 24, Issue 3, Pages 170–172
DOI: https://doi.org/10.1016/j.mencom.2014.04.016
(Mi mendc2513)
 

This article is cited in 15 scientific papers (total in 15 papers)

Communications

Sodium acetate catalyzed multicomponent approach to medicinally privileged 2-amino-4H-chromene scaffold from salicylaldehydes, malononitrile and cyanoacetates

M. N. Elinsona, F. V. Ryzhkova, R. F. Nasybullina, T. A. Zaimovskayab, M. P. Egorova

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Sodium acetate-catalyzed multicomponent assembling of salicylaldehydes, malononitrile and cyanoacetates in water–alcohol mixture (1: 1) at ambient temperature affords alkyl (2-amino-3-cyano-4H-chromen-4-yl)cyanoacetates in 88–95% yields.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (168.1 Kb)


Citation: M. N. Elinson, F. V. Ryzhkov, R. F. Nasybullin, T. A. Zaimovskaya, M. P. Egorov, “Sodium acetate catalyzed multicomponent approach to medicinally privileged 2-amino-4H-chromene scaffold from salicylaldehydes, malononitrile and cyanoacetates”, Mendeleev Commun., 24:3 (2014), 170–172
Linking options:
  • https://www.mathnet.ru/eng/mendc2513
  • https://www.mathnet.ru/eng/mendc/v24/i3/p170
  • This publication is cited in the following 15 articles:
    1. Rahul A Nagarkar, Sudhir E Dapurkar, “Disodium Anacardate: A Bio-based Catalyst for Room Temperature Synthesis of New, Fluorescent 1, 4-Benzoxazinone and Benzophenoxazinone Derivatives”, J Chem Sci, 134:3 (2022)  crossref
    2. Majid Heravi, Vahideh Zadsirjan, Recent Advances in Applications of Name Reactions in Multicomponent Reactions, 2020, 269  crossref
    3. M. N. Elinson, A. N. Vereshchagin, Y. E. Anisina, A. S. Goloveshkin, I. E. Ushakov, M. P. Egorov, “Multicomponent transformation of salicylaldehydes, 2-aminoprop-1-ene-1,1,3-tricarbonitrile, and pyrazolin-5-ones into substituted 2,4-diamino-5-(5-hydroxy-3-methyl-1H-pyrazol-4-yl)-5H-chromeno[2,3-b]pyridine-3-carbonitriles”, Russ Chem Bull, 67:9 (2018), 1695  crossref
    4. Michail N. Elinson, Anatoly N. Vereshchagin, Alexander D. Korshunov, Mikhail P. Egorov, “A fast and efficient 'on-solvent' cascade assembling of salicylaldehydes and dimethylbarbituric acid into 5-(1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-triones”, Heterocyclic Communications, 24:2 (2018), 79  crossref
    5. M. N. Elinson, A. N. Vereshchagin, Yu. E. Anisina, A. S. Goloveshkin, I. E. Ushakov, M. P. Egorov, “PASE facile and efficient multicomponent approach to the new type of 5-C-substituted 2,4-diamino-5H-chromeno[2,3-b]pyridine scaffold”, Mendeleev Commun., 28:4 (2018), 372–374  mathnet  crossref
    6. Majid M. Heravi, Vahideh Zadsirjan, Malihe Mollaiye, Masumeh Heydari, Afsaneh Taheri Kal Koshvandi, “Salicylaldehydes as privileged synthons in multicomponent reactions”, Russian Chem. Reviews, 87:6 (2018), 553–585  mathnet  mathnet  crossref  isi  scopus
    7. M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, A. D. Korshunov, R. A. Novikov, M. P. Egorov, “'On-solvent' new domino reaction of salicylaldehyde, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-one: fast and efficient approach to medicinally relevant 4-pyridinyl-2-amino-4H-chromene scaffold”, Mendeleev Commun., 27:6 (2017), 559–561  mathnet  crossref
    8. Michail N. Elinson, Fedor V. Ryzhkov, Victor A. Korolev, Mikhail P. Egorov, “Pot, atom and step-economic (PASE) synthesis of medicinally relevant spiro[oxindole-3,4′-pyrano[4,3-b]pyran] scaffold”, Heterocyclic Communications, 22:1 (2016), 11  crossref
    9. Michail N. Elinson, Fedor V. Ryzhkov, Ruslan F. Nasybullin, Anatoly N. Vereshchagin, Mikhail P. Egorov, “Fast Efficient and General PASE Approach to Medicinally Relevant 4H,5H‐Pyrano‐[4,3‐b]pyran‐5‐one and 4,6‐Dihydro‐5H‐pyrano‐[3,2‐c]pyridine‐5‐one Scaffolds”, Helvetica Chimica Acta, 99:9 (2016), 724  crossref
    10. M. N. Elinson, F. V. Ryzhkov, A. N. Vereshchagin, T. A. Zaimovskaya, V. A. Korolev, M. P. Egorov, “Multicomponent assembling of isatins, malononitrile and 4-hydroxy-6-methylpyridin-2(1H)-ones: one-pot efficient approach to privileged spiro[indoline-3,4'-pyrano[3,2-c]pyridine]-2,5'(6'H)-dione scaffold”, Mendeleev Commun., 26:5 (2016), 399–401  mathnet  crossref
    11. Anatoly N. Vereshchagin, Michail N. Elinson, Ruslan F. Nasybullin, Fedor V. Ryzhkov, Sergey I. Bobrovsky, Ivan S. Bushmarinov, Mikhail P. Egorov, “One‐Pot 'On‐solvent' Multicomponent Protocol for the Synthesis of Medicinally Relevant 4H‐Pyrano[3,2‐c]quinoline Scaffold”, Helvetica Chimica Acta, 98:8 (2015), 1104  crossref
    12. Yufeng Ren, Wei Zhang, Jun Lu, Kai Gao, Xiali Liao, Xiaozhen Chen, “One-pot synthesis of tetrahydro-4H-chromenes by supramolecular catalysis in water”, RSC Adv., 5:97 (2015), 79405  crossref
    13. Anatoly N. Vereshchagin, Michail N. Elinson, Fedor V. Ryzhkov, Ruslan F. Nasybullin, Sergey I. Bobrovsky, Alexander S. Goloveshkin, Mikhail P. Egorov, “Multicomponent assembling of salicylaldehydes, malononitrile, and 4-hydroxy-6-methyl-2H-pyran-2-one: A fast and efficient approach to medicinally relevant 2-amino-4H-chromene scaffold”, Comptes Rendus. Chimie, 18:12 (2015), 1344  crossref
    14. Michail N. Elinson, Fedor V. Ryzhkov, Anatoly N. Vereshchagin, Sergey V. Gorbunov, Mikhail P. Egorov, “Multicomponent assembling of salicylaldehydes, malononitrile and cyanoacetamides: A simple and efficient approach to medicinally relevant 2-amino-4H-chromene scaffold”, Comptes Rendus. Chimie, 18:5 (2015), 540  crossref
    15. Michail N. Elinson, Fedor V. Ryzhkov, Ruslan F. Nasybullin, Tatiana A. Zaimovskaya, Mikhail P. Egorov, “ChemInform Abstract: Sodium Acetate Catalyzed Multicomponent Approach to Medicinally Privileged 2‐Amino‐4H‐chromene Scaffold from Salicylaldehydes, Malononitrile and Cyanoacetates.”, ChemInform, 45:42 (2014)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Mendeleev Communications
    Statistics & downloads:
    Abstract page:32
    Full-text PDF :6
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025