Organic Letters · 2012 · 29 citations · 53 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisComplex Molecule SynthesisMacrocycle DiversificationMacrocyclic CompoundsMacrocyclic Library ConstructionRing-closing MetathesisRing-forming ReactionsSpirocyclic ScaffoldsSpiroheterocycle Synthesis
The synthesis of two complex subunits en route to spirolide C is described. A key alkyllithium addition to an aldehyde joins the fragments, which are advanced in order to investigate a ring-closing metathesis to form the 23-membered all-carbon macrocyclic framework.
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Tamio Hayashi, Mitsuo Konishi, Yuji Kobori et al. · Journal of the American Chemical Society · 1984 · 747 citations