Proceedings of the Symposium on Progress in Organic Reactions and Syntheses
34th Symposium on Progress in Organic Reactions and Syntheses
Session ID : 1P-45
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AM 11:10~PM 0:22/Poster short talk
Synthetic study of the neuronal cell protecting carbazomadurin A, B
*yuzo hieda
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Abstract
The biologically active carbazole alkaloids, carbazomadurin A and B were isolated from microorganism Actinomadura madurae 2808-SV1 by Seto and co-workers in 1997. These were also shown to be a potent neuronal cell protecting substance which exhibits a free radical scavenging activity. We report the synthesis of the highly substituted carbazole alkaloids, carbazomadurin A and B by the construction of the appropriate carbazole framework based on the allene-mediated electrocyclic reaction of the 6-electron system involving the indole 2,3-bond.
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© 2008 The Pharmaceutical Society of Japan
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