Properties of 3,3-dialkyl-3,4-dihydro-isoquinoline cyclic azomethines

The reactions of 3,3-dialkyl-3,4-dihydroisoquinoline cyclic azomethines with the methyl ester and p-toluidide of iodoacetic acid gave stable quaternary ammonium salts which were suitable dipoles for [3+2] cycloaddition reactions. Azomethines activated by iodomethylation react with potassium cyanide...

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Veröffentlicht in:	Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2009-12, Vol.45 (12), p.1473-1477
Hauptverfasser:	Surikov, O. V., Mikhailovskii, A. G., Vakhrin, M. I.
Format:	Artikel
Sprache:	eng
Schlagworte:	Chemistry Chemistry and Materials Science Organic Chemistry Pharmacy
Online-Zugang:	Volltext
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Beschreibung
Zusammenfassung:	The reactions of 3,3-dialkyl-3,4-dihydroisoquinoline cyclic azomethines with the methyl ester and p-toluidide of iodoacetic acid gave stable quaternary ammonium salts which were suitable dipoles for [3+2] cycloaddition reactions. Azomethines activated by iodomethylation react with potassium cyanide and malonodinitrile.
ISSN:	0009-3122 1573-8353
DOI:	10.1007/s10593-010-0453-x