3-(4-Acylaminopyrazol-5-yl)-4-methylindoles (13a,b), under Bischler-Napieralski reaction conditions, undergo cyclization at the pyrrolic carbon-2 with ultimate formation of the corresponding pyrazolo[3,4:5′,6′]pyrido[3,4-b]indoles (14a,b) as evidenced by crystal structure analysis of 14a.
Received: 2002-8-21
Published Online: 2014-6-2
Published in Print: 2002-11-1
© 1946 – 2014: Verlag der Zeitschrift für Naturforschung
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Keywords for this article
Bischler-Napieralski Reaction;
Directed Cyclization;
Pyrazolopyridoindoles
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