The Journal of Organic Chemistry · 2012 · 27 citations · 23 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistrySynthetic Medicinal ChemistryAnticancer Prodrug DesignMacrocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisAnticancer ActivityMacrocycle DiversificationMacrocycle Library SynthesisMacrocyclic Library SynthesisStereocontrolled Library SynthesisStereoselective Cross-couplingStereoselective MacrocyclizationStereoselective Synthesis
FD-891, a structurally unique 16-membered macrolide having anticancer activity, was synthesized according to a strategy employing asymmetric allylation, Prins cyclization, cross-metathesis reaction, Yamaguchi lactonization, and Julia-Kocienski olefination.
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A General Model for Selectivity in Olefin Cross Metathesis
Arnab Chatterjee, Tae‐Lim Choi, Daniel P. Sanders et al. · Journal of the American Chemical Society · 2003 · 1.5K citations