Synthesis of Pyrazolo- and [1,2,4]triazolo-[1,5-а]quinolin-9-ols by Cycloaddition to 8-Hydroxyquinoline N-imide Full article
| Journal |
Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353 |
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| Output data | Year: 2019, Volume: 55, Number: 3, Pages: 229-234 Pages count : 6 DOI: 10.1007/s10593-019-02446-0 | ||||||
| Tags | 1,3-dipolar cycloaddition; 8-hydroxyquinoline; N-imines; pyrazolo[1,5-а]quinoline; [1,2,4]triazolo[1,5-а]quinoline | ||||||
| Authors |
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| Affiliations |
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Funding (1)
| 1 | Russian Science Foundation | 18-73-00133 |
Abstract:
The reaction of 1-amino-8-hydroxyquinolinium mesitylenesulfonate with alkenes and alkynes containing electron-withdrawing substituents was performed in MeCN–K2СО3 system and gave the respective
9-hydroxypyrazolo[1,5-a]quinolines. The reaction with acetonitrile and aromatic nitriles in aqueous
2 N KОН solution gave the respective 2-substituted 9-hydroxy[1,2,4]triazolo[1,5-a]quinolines.
Cite:
Evtushok V.E.
, Vorob’ev A.Y.
Synthesis of Pyrazolo- and [1,2,4]triazolo-[1,5-а]quinolin-9-ols by Cycloaddition to 8-Hydroxyquinoline N-imide
Chemistry of Heterocyclic Compounds. 2019. V.55. N3. P.229-234. DOI: 10.1007/s10593-019-02446-0 WOS Scopus РИНЦ ANCAN OpenAlex OpenAlex
Synthesis of Pyrazolo- and [1,2,4]triazolo-[1,5-а]quinolin-9-ols by Cycloaddition to 8-Hydroxyquinoline N-imide
Chemistry of Heterocyclic Compounds. 2019. V.55. N3. P.229-234. DOI: 10.1007/s10593-019-02446-0 WOS Scopus РИНЦ ANCAN OpenAlex OpenAlex
Original:
Евтушок В.Е.
, Воробьев А.Ю.
Синтез производных пиразоло- и [1,2,4]триазоло[1,5-а]хинолин-9-олов на основе реакции циклоприсоединения к N-имиду 8-гидроксихинолинa
Химия гетероциклических соединений. 2019. Т.55. №3. С.229–234. РИНЦ
Синтез производных пиразоло- и [1,2,4]триазоло[1,5-а]хинолин-9-олов на основе реакции циклоприсоединения к N-имиду 8-гидроксихинолинa
Химия гетероциклических соединений. 2019. Т.55. №3. С.229–234. РИНЦ
Dates:
| Submitted: | Feb 7, 2019 |
| Accepted: | Feb 24, 2019 |
| Published print: | Mar 1, 2019 |
| Published online: | Apr 23, 2019 |
Identifiers:
| Web of science: | WOS:000467059700008 |
| Scopus: | 2-s2.0-85065392502 |
| Elibrary: | 38690645 |
| Chemical Abstracts: | 2019:840641 |
| Chemical Abstracts (print): | 170:605268 |
| OpenAlex: | W2940826130 | W2942838278 |