Loading [MathJax]/jax/output/SVG/config.js
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, 2010, Volume 20, Issue 5, Pages 288–290
DOI: https://doi.org/10.1016/j.mencom.2010.09.017
(Mi mendc3069)
 

This article is cited in 7 scientific papers (total in 7 papers)

Reaction of 1,3-dimethyl-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)-dione with isatins

S. V. Vasilevskiia, Yu. V. Nelyubinab, N. G. Kolotyrkinaa, P. A. Belyakova, L. B. Kulikovaa, A. N. Kravchenkoa

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 (426 kB) Citations (7)
Abstract: Condensation of 1,3-dimethyl-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)-dione with isatins afforded 6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3,3a,9,9a-tetrahydro-1,3-dimethyl-3a,9a-diphenylimidazo-[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-2,7(1H,6H)-diones; a new conglomerate (space group P212121) was found by an X-ray diffraction study.
Document Type: Article
Language: English


Citation: S. V. Vasilevskii, Yu. V. Nelyubina, N. G. Kolotyrkina, P. A. Belyakov, L. B. Kulikova, A. N. Kravchenko, “Reaction of 1,3-dimethyl-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)-dione with isatins”, Mendeleev Commun., 20:5 (2010), 288–290
Linking options:
  • https://www.mathnet.ru/eng/mendc3069
  • https://www.mathnet.ru/eng/mendc/v20/i5/p288
  • This publication is cited in the following 7 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, A. N. Izmest'ev, “Oxoindolinylidene Derivatives of Thiazolidin-4-ones: Methods of Synthesis and Biological Activity (Review)”, Chem Heterocycl Comp, 50:11 (2015), 1515  crossref
    4. Galina A. Gazieva, Ekaterina A. Shishkova, Ludmila B. Kulikova, Natal'ya G. Kolotyrkina, Natal'ya V. Sigay, Angelina N. Kravchenko, “Diastereoselective Synthesis of (Z)‐6‐(2‐Oxo‐1,2‐dihydro‐3H‐indol‐3‐ylidene)‐3,3a,9,9a‐tetrahydroimidazo[4,5‐e]thiazolo[3,2‐b]‐1,2,4‐triazin‐2,7(1H,6H)‐diones”, Journal of Heterocyclic Chem, 51:4 (2014), 921  crossref
    5. 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  mathnet  crossref
    6. G. A. Gazieva, S. A. Serkov, N. V. Sigai, N. N. Kostikova, Yu. V. Nelyubina, E. A. Shishkova, A. N. Kravchenko, “Synthesis of New Imidazo[4,5-e][1,3]thiazolo-[3,2-b][1,2,4]triazine Derivatives”, Chem Heterocycl Comp, 49:7 (2013), 1097  crossref
    7. Sergei V. Vasilevskii, Yulia V. Nelyubina, Natal'ya G. Kolotyrkina, Pavel A. Belyakov, Lyudmila B. Kulikova, Angelina N. Kravchenko, “ChemInform Abstract: Reaction of 1,3‐Dimethyl‐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)‐dione with Isatins.”, ChemInform, 42:8 (2011)  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:24
    Full-text PDF :5
     
      Contact us:
    math-net2025_03@mi-ras.ru
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025