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Mendeleev Communications, 2019, Volume 29, Issue 4, Pages 369–371
DOI: https://doi.org/10.1016/j.mencom.2019.07.002
(Mi mendc1525)
 

This article is cited in 9 scientific papers (total in 9 papers)

Communications

A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne

S. Gundalaab, M. R. Gudaac, A. F. Khasanovad, D. S. Kopchukad, A. P. Krinochkinad, S. Santraa, G. V. Zyryanovad, P. Venkatapuramb, J. R. Garciac, V. N. Charushinad

a Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation
b Department of Chemistry, Sri Venkateswara University, Andhra Pradesh, India
c Departamento de Química, Universidade Estadual de Ponta Grossa, Paraná, Brazil
d I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Full-text PDF (368 kB) Citations (9)
Abstract: 12-(1H-1,2,3-Triazol-1-yl)indolo[2,1-a]isoquinolines are prepared in 51–56% yields using a PASE (pot, atom, step, economic)-based approach, namely, by the reaction between available 5-R-6-Ar-3-(isoquinolin-1-yl)-1,2,4-triazines and in situ generated benzyne. A mechanism comprising domino-transformation was suggested, and the structure of one key product was confirmed by a single crystal X-ray diffraction analysis.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (909.6 Kb)


Citation: S. Gundala, M. R. Guda, A. F. Khasanov, D. S. Kopchuk, A. P. Krinochkin, S. Santra, G. V. Zyryanov, P. Venkatapuram, J. R. Garcia, V. N. Charushin, “A PASE-based approach towards 12-(1H-1,2,3-triazol-1-yl)-indolo[2,1-a]isoquinolines via the reaction of 3-(isoquinolin-1-yl)-1,2,4-triazines with benzyne”, Mendeleev Commun., 29:4 (2019), 369–371
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  • https://www.mathnet.ru/eng/mendc/v29/i4/p369
  • This publication is cited in the following 9 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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