Journal of the American Chemical Society · 2007 · 78 citations · 16 references
Medicinal ChemistryModified Stille CouplingBioorganic ChemistryBiochemistryNatural SciencesMedicineTotal SynthesisOrganic ChemistrySelective V-atpase InhibitorStereoselective SynthesisChemistryArchazolid BHeterocycle ChemistryPharmacologySynthetic ChemistryDrug DiscoveryNatural Product Synthesis
A highly convergent synthesis of archazolid B, a potent and highly selective V-ATPase inhibitor, is described. A relay ring-closing metathesis reaction was used to form the 24-membered macrocyclic lactone, whereas the sensitive cis-triene moiety of the archazolids was assembled with a modified Stille coupling.
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On the Nature of the "Copper Effect" in the Stille Cross-Coupling
Vittorio Farina, Suresh Kapadia, Bala Krishnan et al. · The Journal of Organic Chemistry · 1994 · 501 citations
Herbert C. Brown, K. S. BHAT · Journal of the American Chemical Society · 1986 · 376 citations
Engineering, Threo-.beta.-methylhomoallyl Alcohols, Natural Sciences +14