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Mendeleev Communications, 2012, Volume 22, Issue 2, Pages 90–91
DOI: https://doi.org/10.1016/j.mencom.2012.03.013
(Mi mendc2750)
 

This article is cited in 5 scientific papers (total in 5 papers)

[3 + 2]-Cycloaddition of azomethine ylide at 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones

A. N. Kravchenkoa, P. A. Poluboyarova, S. V. Vasilevskiia, G. A. Gazievaa, Yu. V. Nelyubinab

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (295 kB) Citations (5)
Abstract: [3 + 2]-Cycloaddition of azomethine ylide generated from formaldehyde and sarcosine at the double bond of 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones occurs stereospecifically at the face opposite to the phenyl substituents. Product 3a crystallizes as a conglomerate.
Document Type: Article
Language: English


Citation: A. N. Kravchenko, P. A. Poluboyarov, S. V. Vasilevskii, G. A. Gazieva, Yu. V. Nelyubina, “[3 + 2]-Cycloaddition of azomethine ylide at 1,3-dimethyl-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e][1,3]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-diones”, Mendeleev Commun., 22:2 (2012), 90–91
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  • https://www.mathnet.ru/eng/mendc2750
  • https://www.mathnet.ru/eng/mendc/v22/i2/p90
  • This publication is cited in the following 5 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. G. A. Gazieva, N. G. Kolotyrkina, A. N. Kravchenko, N. N. Makhova, “Synthesis of novel spiro[indole-3,3′-pyrrolidin]-2(1H)-ones”, Russ Chem Bull, 63:2 (2014), 431  crossref
    4. Angelina N. Kravchenko, Pavel A. Poluboyarov, Sergei V. Vasilevskii, Galina A. Gazieva, Yulia Y. Nelyubina, “ChemInform Abstract: [3 + 2]‐Cycloaddition of Azomethine Ylide at 1,3‐Dimethyl‐6‐ (2‐oxo‐1,2‐dihydro‐3H‐indol‐3‐ylidene) ‐3a,9a‐diphenyl‐3,3a,9,9a‐tetrahydroimidazo[4,5‐e][1,3]thiazolo[3,2‐b] [1,2,4]triazine‐2,7(1H,6H)‐diones.”, ChemInform, 43:35 (2012)  crossref
    5. G. A. Gazieva, P. A. Poluboyarov, Yu. V. Nelyubina, M. I. Struchkova, A. N. Kravchenko, “Synthesis of imidazo[4,5-e][1,3]thiazolo-[3,2-b][1,2,4]triazines”, Chem Heterocycl Comp, 48:9 (2012), 1382  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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