Organic Letters · 2001 · 66 citations · 15 references
PharmacyChemistryMedicinal ChemistryNatural Product BiosynthesisSynthetic Medicinal ChemistryAlkaloid BiosynthesisPlant Natural Product BiosynthesisRetrosynthetic AnalysisAlkaloid Skeleton FormationBiosynthetic Intermediates In Alkaloid PathwaysIminium IonsNatural Product Total SynthesisPlant AlkaloidsPurine Alkaloid BiosynthesisRing-closing MetathesisTotal Synthesis-derived Analogues
[structure: see text]. The concise total synthesis of securinine in nine steps from readily available starting materials is described. Key steps of the synthesis include an addition of a silyloxyfuran to an in situ generated iminium ion and a novel ring closing metathesis reaction.
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Peter Schwab, Marcia B. France, Joseph W. Ziller et al. · Angewandte Chemie International Edition in English · 1995 · 1.5K citations
Securinine alkaloids: A new class of GABA receptor antagonist
John A. Beutler, E. William Karbon, Abram N. Brubaker et al. · Brain Research · 1985 · 127 citations