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Synthesis 2006(8): 1375-1385
DOI: 10.1055/s-2006-926410
DOI: 10.1055/s-2006-926410
FEATUREARTICLE
© Georg Thieme Verlag Stuttgart · New York
The Palladium-Catalyzed Preparation of Condensed Tetracyclic Heterocycles and their Application to the Synthesis of rac-Mangochinine
Further Information
Publication History
Received
11 January 2006
Publication Date:
28 March 2006 (online)


Abstract
Dihydroisoquinoline derivatives and their analogues, prepared by the Bischler-Napieralsky reaction, were converted to their indole-fused derivatives. Scope and limitations of the palladium-catalyzed reaction, proceeding through the tautomeric enamine forms of these compounds, were studied and the process was extended to the preparation of racemic mangochinine.
Key words
ring closure - palladium - catalysis - indoles - natural products