The First Case of an Aryl Imination Reaction by Direct Nucleophilic Substitution of Hydrogen: Synthesis of 2-arylimino Derivatives for 1,2-dihydro-1-methyl-5(6,7,8)-nitroquinolines

The oxidative SNH aryl imination of 1-methyl nitro quinolinium salts is described. The first 2-arylimino derivatives of 1,2-dihydro-1-methyl-5(6,7,8)-nitroquinolines have been synthesized in a one-step reaction (ONSH process) under mild conditions and without preliminary introduction of a leaving gr...

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Hlavní autoři:	Pobedinskaya, D. Y., Побединская, Д. Ю., Demidov, O. P., Демидов, О. П., Ermolenko, A. P., Ермоленко, А. П., Avakyan, E. K., Авакян, Е. К., Borovleva, A. A., Боровлева, А. А., Larin, A. N., Ларин, А. Н., Borovlev, I. V., Боровлев, И. В.
Médium:	Статья
Jazyk:	English
Vydáno:	John Wiley and Sons Inc 2025
Témata:	Heterocyclic imines ONSH process Imination reactions Nucleophilic substitution of hydrogen Quinoline salts
On-line přístup:	https://dspace.ncfu.ru/handle/123456789/30368
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The First Case of an Aryl Imination Reaction by Direct Nucleophilic Substitution of Hydrogen: Synthesis of 2-arylimino Derivatives for 1,2-dihydro-1-methyl-5(6,7,8)-nitroquinolines

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