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http://elar.urfu.ru/handle/10995/101795
Title: | Synthesis, photophysical and redox properties of the 2,5,7-tri(het)aryl- [1,2,4]triazolo[1,5-a]pyrimidines |
Authors: | Rasputin, N. A. Demina, N. S. Irgashev, R. A. Shchepochkin, A. V. Rusinov, G. L. Chupakhin, O. N. Charushin, V. N. |
Issue Date: | 2020 |
Publisher: | Arkat |
Citation: | Synthesis, photophysical and redox properties of the 2,5,7-tri(het)aryl- [1,2,4]triazolo[1,5-a]pyrimidines / N. A. Rasputin, N. S. Demina, R. A. Irgashev, et al. — DOI 10.24820/ARK.5550190.P011.247 // Arkivoc. — 2020. — Vol. 2020. — Iss. 6. — P. -. |
Abstract: | A number of Y-type push-pull compounds based on the [1,2,4]triazolo[1,5-a]pyrimidine core, namely 5,7- di(het)aryl-substituted 2-phenyl-[1,2,4]triazolo[1,5-a]pyrimidines, were obtained by transition metal free nucleophilic C-H functionalization. Substituents at both the C-5 and C-7 positions were introduced by successive treatment of the starting 6-bromo-2-phenyl-[1,2,4]triazolo[1,5-a]pyrimidine with Grignard reagents. In addition, the optical and electrochemical properties of the synthesized push-pull systems were studied. © 2020 Arkat. All rights reserved. |
Keywords: | DIRECT (HET)ARYLATION GRIGNARD REAGENTS NUCLEOPHILIC AROMATIC SUBSTITUTION OF HYDROGEN (SNH) [1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE |
URI: | http://elar.urfu.ru/handle/10995/101795 |
Access: | info:eu-repo/semantics/openAccess |
SCOPUS ID: | 85094152481 |
WOS ID: | 000584517600029 |
PURE ID: | 836416af-929e-4171-9462-13f3fffc1ea9 20125521 |
ISSN: | 15517004 |
DOI: | 10.24820/ARK.5550190.P011.247 |
metadata.dc.description.sponsorship: | This research study was supported financially by the Russian Science Foundation (Project No. 19-13-00234). |
RSCF project card: | 19-13-00231 |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
Files in This Item:
File | Description | Size | Format | |
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2-s2.0-85094152481.pdf | 1,11 MB | Adobe PDF | View/Open |
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