Publication | Closed Access
Total synthesis of rutamycin B via Suzuki macrocyclization
21
Citations
8
References
1998
Year
Ring ClosureMedicinal ChemistryMacrolide Rutamycin BBiochemistryNatural SciencesMedicineSuzuki MacrocyclizationStereoselective SynthesisVinyl–vinyl CouplingPharmacologySynthetic ChemistryDrug DiscoveryNatural Product Synthesis
The macrolide rutamycin B containing 17 stereogenic centres and a 26-membered ring was synthesized by a route which features a chelate-controlled, double differentiating aldol reaction and ring closure by means of a vinyl–vinyl coupling.
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