Angewandte Chemie International Edition · 2022 · 30 citations · 55 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAlkaloid BiosynthesisDiversity-oriented SynthesisAsymmetric SynthesisCore Scaffold LibrariesEnantioselective SynthesisIndole AlkaloidsIndole ChemistryIndole DerivativesIndole SynthesisPlant Alkaloids
We report an intramolecular conjugate addition/Truce-Smiles/E1cb cascade of 2-nitrobenzenesulfonamide-functionalized cyclohexenones as a new entry to the core scaffold of monoterpene indole alkaloids. The method was applied to the asymmetric total synthesis of (-)-limaspermidine, (-)-kopsinilam, and (-)-kopsinine, as well as the framework of the kopsifoline alkaloids, thus highlighting its complementarity to existing approaches involving the use of indole-based starting materials or the interrupted Fischer indole synthesis. Furthermore, we show that the cascade tolerates various substituents on the nitroarene, opening the way to other natural products as well as non-natural analogues.
55
Collective synthesis of natural products by means of organocascade catalysis
Spencer B. Jones, Bryon Simmons, Anthony Mastracchio et al. · Nature · 2011 · 731 citations
THE TOTAL SYNTHESIS OF STRYCHNINE
R. B. Woodward, Michael P. Cava, W. David Ollis et al. · Journal of the American Chemical Society · 1954 · 316 citations
Sergey A. Kozmin, Tetsuo Iwama, Yong Huang et al. · Journal of the American Chemical Society · 2002 · 284 citations