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Mendeleev Communications, 2014, Volume 24, Issue 2, Pages 119–121
DOI: https://doi.org/10.1016/j.mencom.2014.03.019
(Mi mendc2493)
 

This article is cited in 8 scientific papers (total in 8 papers)

Communications

Cascade synthesis of the first imidazo[4,5-e]-thiazolo[2,3-c][1,2,4]triazine derivative

A. N. Kravchenkoa, G. A. Gazievaa, S. V. Vasilevskiib, Yu. V. Nelyubinac

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (357 kB) Citations (8)
Abstract: (Z)-7-(3,5-Di-tert-butyl-6-oxocyclohexa-2,4-dien-1-ylidene)-1,3-dimethyl-3a,9a-diphenyl-1,3a,4,9a-tetrahydroimidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazine-2,8(3H,7H)-dione was obtained by aldol condensation of 3,5-di-tert-butyl-1,2-benzoquinone with 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-dione followed by intramolecular thiazole ring-opening/closing in the condensation primary adduct.
Document Type: Article
Language: English


Citation: A. N. Kravchenko, G. A. Gazieva, S. V. Vasilevskii, Yu. V. Nelyubina, “Cascade synthesis of the first imidazo[4,5-e]-thiazolo[2,3-c][1,2,4]triazine derivative”, Mendeleev Commun., 24:2 (2014), 119–121
Linking options:
  • https://www.mathnet.ru/eng/mendc2493
  • https://www.mathnet.ru/eng/mendc/v24/i2/p119
  • This publication is cited in the following 8 articles:
    1. S.M. Ivanov, Comprehensive Heterocyclic Chemistry IV, 2022, 29  crossref
    2. N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Russian Chem. Reviews, 89:1 (2020), 55–124  mathnet  mathnet  crossref  isi  scopus
    3. Chita R. Sahoo, Sudhir K. Paidesetty, Rabindra N. Padhy, “Nornostocine congeners as potential anticancer drugs: An overview”, Drug Development Research, 80:7 (2019), 878  crossref
    4. Galina A. Gazieva, Alexei N. Izmest'ev, Lada V. Anikina, Sergey A. Pukhov, Marina E. Meshchaneva, Dmitry V. Khakimov, Natalya G. Kolotyrkina, Angelina N. Kravchenko, “The influence of substituents on the reactivity and cytotoxicity of imidazothiazolotriazinones”, Mol Divers, 22:3 (2018), 585  crossref
    5. Angelina N. Kravchenko, Sergei V. Vasilevskii, Galina A. Gazieva, Vladimir V. Baranov, Valery A. Barachevsky, Olga I. Kobeleva, Olga V. Venidiktova, Valentina A. Karnoukhova, “Transformations of S-substituted 5,7-dimethyl-4a,5a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-2-ones under treatment of 1,2-benzoquinones and photochemical properties of reaction products”, Tetrahedron, 74:19 (2018), 2359  crossref
    6. Galina A. Gazieva, Alexei N. Izmest'ev, Yulia V. Nelyubina, Natalya G. Kolotyrkina, Igor E. Zanin, Angelina N. Kravchenko, “Synthesis of imidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazine-2,8-diones via a rearrangement of imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-2,7-diones in the reaction with isatins”, RSC Adv., 5:55 (2015), 43990  crossref
    7. A. N. Kravchenko, S. V. Vasilevskii, G. A. Gazieva, Yu. V. Nelyubina, “Unexpected formation of 6-[benzofuran-3(2H)-ylidene]-3,3a,9,9a-tetra-hydroimidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazine-2,7-dione derivative”, Mendeleev Commun., 25:6 (2015), 476–478  mathnet  crossref
    8. Angelina N. Kravchenko, Galina A. Gazieva, Sergei V. Vasilevskii, Yulia V. Nelyubina, “ChemInform Abstract: Cascade Synthesis of the First Imidazo[4,5‐e]thiazolo[2,3‐c][1,2,4]triazine Derivative (IV).”, ChemInform, 45:37 (2014)  crossref
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