Angewandte Chemie International Edition · 2022 · 11 citations · 36 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoverySynthetic Medicinal ChemistryAnalog DesignEnzyme InhibitionAnalog IsolationBioactive Molecule SynthesisChemical Synthesis Of AnaloguesConjugate AdditionEnzyme Inhibitor SynthesisFragment Coupling StrategyNovel Analogue GenerationSynthetic Analogues
We report a concise synthesis of the naturally occurring protein synthesis inhibitor (+)-actinobolin (1). The densely functionalized and stereochemically complex molecular structure of 1 was assembled from (-)-quinic acid, L-threonine, and L-alanine as the principal components. Our route is based around a convergent strategy that features conjugate addition of an α-amino radical in the key fragment-coupling step. The dramatically simplified synthesis of (+)-actinobolin proceeding in 9 steps with 18 % overall yield has practical implications for analog preparation, as demonstrated herein.
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Filippo Sladojevich, Andrea Trabocchi, Antonio Guarna et al. · Journal of the American Chemical Society · 2011 · 256 citations