11 citations to 10.1070/MC2002v012n02ABEH001560 (Crossref Cited-By Service)
  1. Antonio Guirado, José I. López Sánchez, Delia Bautista, “Reactions of 5,8-dichloro-2,3-dicyanoquinoxaline with amines and hydrazines. A new and efficient synthetic approach to 3-amino-5,8-dichloroflavazoles”, Tetrahedron, 67, no. 22, 2011, 4123  crossref
  2. Hui Tang, Juan Wu, Wen Zhang, Lei Zhao, Ya-Hui Zhang, Cheng-Wu Shen, “Design, synthesis and biological evaluation of novel non-azole derivatives as potential antifungal agents”, Chinese Chemical Letters, 26, no. 9, 2015, 1161  crossref
  3. Anna V. Gulevskaya, Alexander F. Pozharskii, 93, Advances in Heterocyclic Chemistry Volume 93, 2007, 57  crossref
  4. Michael P. Groziak, 15, A critical review of the 2002 fiterature preceded by three chapters on current heterocyclic topics, 2003, 306  crossref
  5. S. K. Kotovskaya, V. N. Charushin, N. M. Perova, M. I. Kodess, O. N. Chupakhin, “Intramolecular Nucleophilic Substitution of Hydrogen in (Quinoxalinyl‐2)aminovinyl Derivatives as a New Approach to Pyrrolo‐ and Indolo[2,3‐b]quinoxalines”, Synthetic Communications, 34, no. 14, 2004, 2531  crossref
  6. A. M. Boguslavskii, M. G. Ponizovskii, M. I. Kodess, V. N. Charushin, “Ring-Chain Transformations of Dihydroisoxazolo[4,5-b]quinoxaline”, Russ J Org Chem, 41, no. 9, 2005, 1377  crossref
  7. Michail G. Ponizovsky, Artem M. Boguslavsky, Mikhail I. Kodess, Valery N. Charushin, Oleg N. Chupakhin, “Synthesis of Fused Quinoxalines.”, ChemInform, 33, no. 39, 2002, 163  crossref
  8. Valery N. Charushin, Oleg N. Chupakhin, 37, Metal Free C-H Functionalization of Aromatics, 2014, 1  crossref
  9. Yuriy A. Kvashnin, Egor V. Verbitskiy, Ekaterina F. Zhilina, Gennady L. Rusinov, Oleg N. Chupakhin, Valery N. Charushin, “Synthesis of Heteroannulated Indolopyrazines through Domino N–H Palladium-Catalyzed/Metal-Free Oxidative C–H Bond Activation”, ACS Omega, 5, no. 25, 2020, 15681  crossref
  10. Valery N. Charushin, Oleg N. Chupakhin, “Nucleophilic aromatic substitution of hydrogen and related reactions”, Mendeleev Communications, 17, no. 5, 2007, 249  crossref
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