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Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

European Journal of Organic Chemistry · 2003 · Vol. 2003(12) · pp. 2209–2219
Christiane MartiErick M. Carreira

Abstract

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)

Chemical synthesis and alkaloidsAsymmetric Synthesis and CatalysisAlkaloids: synthesis and pharmacologyPyrrolidineOxindoleChemistryRing (chemistry)Context (archaeology)Chemical synthesisStereochemistryTotal synthesisCombinatorial chemistryOrganic chemistry
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References
Rules for ring closure
Journal of the Chemical Society Chemical Communications · 1976 · 2,224 citations
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