European Journal of Organic Chemistry · 2003 · 1.4K citations · 106 references
PharmacyChemistryMedicinal ChemistryDrug DesignDrug DiscoverySynthetic Medicinal ChemistryAlkaloid BiosynthesisHeterocycle SynthesisRetrosynthetic AnalysisBiological Activity FeaturesPyrrolidine AlkaloidsSpirocyclic Scaffolds
Abstract The spiro[pyrrolidine‐3,3′‐oxindole] ring system is found at the core of a number of alkaloids, which possess significant biological activity and are interesting, challenging targets for chemical synthesis. In the present review, we report on the different strategies for the synthesis of the spiro[pyrrolidine‐3,3′‐oxindole] ring system in the context of recent synthesis of coerulescine, horsfiline, elacomine, salacin, pteropodine, alstonisine, spirotryprostatin A and B, and strychnofoline. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
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Jack E. Baldwin · Journal of the Chemical Society Chemical Communications · 1976 · 2.2K citations
Horsfiline, an oxindole alkaloid from Horsfieldia superba
Akino Jössang, Per Jossang, Hamid Hadi et al. · The Journal of Organic Chemistry · 1991 · 418 citations