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Synthesis 2002(3): 0323-0325
DOI: 10.1055/s-2002-20047
DOI: 10.1055/s-2002-20047
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York
Biogenetic Synthesis of Luotonin F [1]
Further Information
Received
30 November 2001
Publication Date:
28 July 2004 (online)
Publication History
Publication Date:
28 July 2004 (online)
Abstract
Three-step biogenetic type synthesis of recently isolated bioactive natural product Luotonin F (1) with 38% overall yield has been described starting from the natural product pegamine (4a) via PCC-oxidation, Friedländer condensation, and chromium trioxide-periodic acid oxidation reactions.
Key words
pegamine - PCC-oxidation - o-aminobenzaldehyde - Friedländer condensation - Luotonin F synthesis
NCL Communication No. 6618.
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References
NCL Communication No. 6618.