Synthesis Of 2-Acyltetrahydro-β-Carbolines By An Intramolecular α-Amidoalkylation Reaction

2-Acyltetrahydro-β-carbolines 7 have been obtained by cyclization of adducts 5 from imines 3 of tryptamine 1 and aldehydes 2 with acyl chlorides 4 as a result of an intramolecular a-amidoalkylation reaction in the presence of bases as N,N-dimethylaniline or Et 3 N.

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Veröffentlicht in:Synthetic communications 1999-02, Vol.29 (3), p.487-494
Hauptverfasser: Venkov, Atanas P., Boyadjieva, Atanaska K.
Format: Artikel
Sprache:eng
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Zusammenfassung:2-Acyltetrahydro-β-carbolines 7 have been obtained by cyclization of adducts 5 from imines 3 of tryptamine 1 and aldehydes 2 with acyl chlorides 4 as a result of an intramolecular a-amidoalkylation reaction in the presence of bases as N,N-dimethylaniline or Et 3 N.
ISSN:0039-7911
1532-2432
DOI:10.1080/00397919908085791