Organic Letters · 2012 · 40 citations · 21 references
PharmacyChemistryMedicinal ChemistryCatalysisDrug DiscoverySynthetic Medicinal ChemistryDiversity-oriented SynthesisLigand-based DesignOrganic SynthesisDiversity-oriented Heterocycle SynthesisHeterocycle FunctionalizationLactam SynthesisPyrrolidine SynthesisScaffold SynthesisScaffold-based Library SynthesisSite-selective FunctionalizationSpirocyclic Scaffolds
Expedient routes to three classes of novel spiro-fused pyrrolidine, piperidine, and indoline heterocycle scaffolds are described. These three-dimensional frameworks, which conform to the "rule of three", are suitably protected to allow for site-selective manipulation and functionalization. Different modes of substrate control were explored, which allow for good to excellent levels of diastereoselectivity and dispense with the need for additional chiral reagents or catalysts. The concepts developed were applied in short, formal syntheses of (±)-coerulescine and (±)-horsfiline.
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Horsfiline, an oxindole alkaloid from Horsfieldia superba
Akino Jössang, Per Jossang, Hamid Hadi et al. · The Journal of Organic Chemistry · 1991 · 418 citations
Marco Bella, Sara Kobbelgaard, Karl Anker Jørgensen · Journal of the American Chemical Society · 2005 · 187 citations
Manzamine alkaloids, syntheses and synthetic approaches
Emmanuel Magnier, Yves Langlois · Tetrahedron · 1998 · 149 citations