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Mendeleev Communications, 2004, Volume 14, Issue 1, Pages 38–39
DOI: https://doi.org/10.1070/MC2004v014n01ABEH001860
(Mi mendc3797)
 

This article is cited in 13 scientific papers (total in 13 papers)

Synthesis of highly functionalised 2-aminofurans

I. Yavari, H. Djahaniani, L. Moradi

Department of Chemistry, Tarbiat Modarres University, Tehran, Iran
Full-text PDF (65 kB) Citations (13)
Abstract: The reaction of alkyl isocyanides and dimethyl 2-oxo-3-arylidenesuccinates leads to highly functionalised aminofuran derivatives in good yields.
Document Type: Article
Language: English


Citation: I. Yavari, H. Djahaniani, L. Moradi, “Synthesis of highly functionalised 2-aminofurans”, Mendeleev Commun., 14:1 (2004), 38–39
Linking options:
  • https://www.mathnet.ru/eng/mendc3797
  • https://www.mathnet.ru/eng/mendc/v14/i1/p38
  • This publication is cited in the following 13 articles:
    1. Shirin Sharafian, Zinatossadat Hossaini, Faramarz Rostami-Charati, Mohammad A. Khalilzadeh, “Green synthesis of novel phosphonate derivatives using ultrasonic irradiation”, Chem Heterocycl Comp, 56:10 (2020), 1283  crossref
    2. Weijian Ye, Chen Tan, Juan Yao, Shuwen Xue, Yang Li, Cunde Wang, “Iodine‐Promoted Domino Reactions of 1‐Cyanocyclopropane 1‐Esters: A Straightforward Approach to Fully Substituted 2‐Aminofurans”, Adv Synth Catal, 358:3 (2016), 426  crossref
    3. Bagher Eftekhari-Sis, Maryam Zirak, “Chemistry of α-Oxoesters: A Powerful Tool for the Synthesis of Heterocycles”, Chem. Rev., 115:1 (2015), 151  crossref
    4. Ana G. Neo, Ana Bornadiego, Jesús Díaz, Stefano Marcaccini, Carlos F. Marcos, “Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines”, Org. Biomol. Chem., 11:38 (2013), 6546  crossref
    5. Morteza Shiri, Majid M. Heravi, Bita Soleymanifard, “Arylidene pyruvic acids (APAs) in the synthesis of organic compounds”, Tetrahedron, 68:33 (2012), 6593  crossref
    6. Ana G. Neo, Jesús Díaz, Stefano Marcaccini, Carlos F. Marcos, “Conjugate addition of isocyanides to chromone 3-carboxylic acid: an efficient one-pot synthesis of chroman-4-one 2-carboxamides”, Org. Biomol. Chem., 10:17 (2012), 3406  crossref
    7. Issa Yavari, Zinatossadat Hossaini, Maryam Sabbaghan, “Synthesis and Dynamic NMR Study of Functionalized 1-(3-Furyl)-1H-indole-2,3-diones”, Monatsh. Chem., 138:2 (2007), 107  crossref
    8. Issa Yavari, Anvar Mirzaei, Loghman Moradi, Ako Mokhtarporiani‐Sanandaj, “Efficient Synthesis of Trialkyl (E)‐3‐{3‐Oxo‐2‐3,4‐dihydro‐2‐(1H)‐quinoxalinylidene}‐prop‐1‐ene‐1,2,3‐tricarboxylates”, Synthetic Communications, 37:7 (2007), 1195  crossref
    9. Heiner Eckert, Alfons Nestl, Ivar Ugi, Carlos F. Marcos, Ana G. Neo, Susana Barriga, Encyclopedia of Reagents for Organic Synthesis, 2006  crossref
    10. I. Yavari, B. Mohtat, H. Zare, “Synthesis of 4,5-dialkyl 5-acetyl-3-oxo-3-(triphenylphosphoranylidene)- tetrahydrofuran-4,5-dicarboxylates”, Mendeleev Commun., 16:2 (2006), 102–104  mathnet  crossref
    11. I. Yavari, M. Sirouspour, S. Souri, F. Nasiri, H. Djahaniani, “Synthesis of 3-alkylidene-1,2,3,5,6,7-hexahydro-4H-indol-4-one derivatives in the THF–H2O system”, Mendeleev Commun., 15:3 (2005), 120–121  mathnet  crossref
    12. Issa Yavari, Hoorieh Djahaniani, Loghman Moradi, “Synthesis of Highly Functionalized 2‐Aminofurans”, ChemInform, 35:33 (2004)  crossref
    13. I. Yavari, H. Djahaniani, F. Nasiri, “Synthesis of highly functionalised 1H-furo[3,4-b]chromenes”, Mendeleev Commun., 14:5 (2004), 214–215  mathnet  crossref
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