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Mendeleev Communications, 2022, Volume 32, Issue 6, Pages 722–725
DOI: https://doi.org/10.1016/j.mencom.2022.11.005
(Mi mendc778)
 

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

Communications

First synthesis of new polycyclic systems from ortho-di(heteroaryl)-substituted furazanopyrazine derivatives by the Scholl reaction

E. V. Verbitskiyab, Yu. A. Kvashninab, M. V. Medvedevab, T. S. Svalovab, A. N. Kozitsinab, O. S. Eltsovb, G. L. Rusinovab, V. N. Charushinab

a I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation
Abstract: A facile synthetic protocol to hard-to-get polycyclic (hetero)-aromatic compounds annulated to [1,2,4]oxadiazolo[3,4-b]-pyrazine scaffold via the FeCl3-mediated intramolecular Scholl cross-coupling has been developed. Based on the electrochemical and photophysical measurements, the synthesized polycyclic systems may be regarded as narrow band-gap (from 1.42 to 1.89 eV) n-type organic semiconductors whose energy levels are comparable to those of the commercially available n-type semiconductors
Keywords: furazanopyrazines, Scholl reaction, organic semiconductors, C–H functionalization, SH-reaction, polycyclic aromatic, hydrocarbons, iron trichloride.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.4 Mb)


Citation: E. V. Verbitskiy, Yu. A. Kvashnin, M. V. Medvedeva, T. S. Svalova, A. N. Kozitsina, O. S. Eltsov, G. L. Rusinov, V. N. Charushin, “First synthesis of new polycyclic systems from ortho-di(heteroaryl)-substituted furazanopyrazine derivatives by the Scholl reaction”, Mendeleev Commun., 32:6 (2022), 722–725
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  • This publication is cited in the following 8 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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