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Total Synthesis of (+)-Fastigiatine
Gretchen Peters February 10, 2011
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Shair Research Group Total synthesis and chemical biology
Focus of syntheses: “naturally occurring complex molecules that challenge the state- of-the-art of organic synthesis” Complexes that are unique structurally and biologically
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Lycopodium alkaloids Found in plants (clubmosses)
(-)-himeradine A lycodine (+)-fastigiatine Found in plants (clubmosses) Members have been found to have cardiovascular and neuromuscular effects Used for homeopathic remedies
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Retrosynthesis 1,4 Addition Mannich Condensation
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Protection 2 1
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Cuperate Addition 2 3
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Alkylation, Decarboxylation
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Addition of Li-enolate
5 7 6
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Intramolecular Aza-Wittig
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Reactive Amine Wanted to remove protecting group and induce addition
Free amine too reactive Added on to a,b unsaturated ketone to form five-membered ring 7
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Acid catalyzed cyclization
7 8 9
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Mannich Reaction 9 10
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Conclusions First synthesis of (+)-fastigiatine
15 step synthesis with 30% overall yield
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Acknowledgements Chem 647 classmates Dr. Davis
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