Synthesis of pyrrolo1,2-aquinolines by formal 1,3-dipolar cycloaddition reactions of quinolinium salts

Quinolinium salts, Q+-CH2-CO2Me Br- and Q+-CH2-CONMe2 Br- (where Q = quinoline), were prepared from quinolines. Deprotonation of these salts with triethylamine promoted the reaction of the resulting quinolinium ylides (formally azomethine ylides) with electron-poor alkenes by conjugate addition foll...

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Veröffentlicht in:	Beilstein journal of organic chemistry 2019-01, Vol.15, p.1480
Hauptverfasser:	Choi, Anthony, Morley, Rebecca M, Coldham, Iain
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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