Domino reactions of 1-substituted N-(cyanomethyl)isoquinolinium salts with salicylic aldehydes

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3267

Title:	Domino reactions of 1-substituted N-(cyanomethyl)isoquinolinium salts with salicylic aldehydes
Authors:	Aksenov, A. V. Аксенов, А. В.
Keywords:	Domino reaction;Isoquinoline;Quaternary salts;Salicylic aldehyde
Issue Date:	2016
Publisher:	Springer New York LLC
Citation:	Voskressensky, L.G., Sokolova, E.A., Festa, A.A., Enina, D.A., Aksenov, A.V., Varlamov, A.V. Domino reactions of 1-substituted N-(cyanomethyl)isoquinolinium salts with salicylic aldehydes // Chemistry of Heterocyclic Compounds. - 2016. - Volume 52. - Issue 6. - Pages 415-420
Series/Report no.:	Chemistry of Heterocyclic Compounds
Abstract:	Transformations of N-cyanomethyl-substituted 1-methyl- and 1-phenylisoquinolinium salts were studied in the presence of various o-hydroxybenzaldehydes, leading to the formation of substituted chromeno[2',3':4,5]imidazo[2,1-a]isoquinolines. 1,8-Diazabicyclo- [5.4.0]undec-7-ene was shown to be a superior base in this reaction compared to sodium carbonate
URI:	http://hdl.handle.net/20.500.12258/3267
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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