Synthesis of 6-Amino-3,4-dihydroisoquinolinium Derivatives by Ring-Opening Reactions of Acridizinium Ions

The reaction of the 9-fluoroacridizinium (9-fluorobenzo[b]quinolizinium) or the 9-aminoacridizinium (9-aminobenzo[b]quinolizinium) ion with primary alkyl amines gives with high diastereoselectivity 6-amino-3,4-dihydroisoquinolinium derivatives as main products, which exhibit pronounced absorption an...

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Veröffentlicht in:Organic letters 2008-03, Vol.10 (5), p.757-760
Hauptverfasser: Deiseroth, Hans-Jörg, Granzhan, Anton, Ihmels, Heiko, Schlosser, Marc, Tian, Maoqun
Format: Artikel
Sprache:eng
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Zusammenfassung:The reaction of the 9-fluoroacridizinium (9-fluorobenzo[b]quinolizinium) or the 9-aminoacridizinium (9-aminobenzo[b]quinolizinium) ion with primary alkyl amines gives with high diastereoselectivity 6-amino-3,4-dihydroisoquinolinium derivatives as main products, which exhibit pronounced absorption and fluorescence properties. It is proposed that the reaction proceeds via a nucleophilic ring-opening followed by an aza Diels−Alder reaction.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol702792r