Organic Letters · 2003 · 107 citations · 20 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryChemical Library DesignCombinatorial SynthesisDiversity-oriented SynthesisMacrocycle SynthesisNatural Product Drug DiscoveryOrganic SynthesisMacrocycle Library SynthesisMacrocyclic CompoundsMacrocyclic Library ConstructionMacrocyclic Library SynthesisMacrocyclic Natural ProductsMulticomponent Reaction ChemistryNatural Product Macrocycle SynthesisRing-closing Metathesis
[reaction: see text] A general strategy toward macrocyclic compounds using multicomponent reaction (MCR) chemistry, e.g., Passerini and Ugi variants, and ring-closing metathesis (RCM) is introduced. The corresponding bifunctional isocyanides carboxylic acids bearing a terminal olefin are easy to prepare from the corresponding commercially available starting materials. Advantageously, this strategy allows fast access to a diverse conformational space of natural product-like macrocycles and could thus be of interest in the discovery of novel bioactive agents.
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Maximizing Synthetic Efficiency: Multi-Component Transformations Lead the Way
Hugues Bienaymé, Chris Hulme, G. ODDON et al. · Chemistry - A European Journal · 2000 · 1.1K citations · Full text
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