Publication | Closed Access
Application of hitherto unexplored macrocyclization strategies in the epothilone series: novel epothilone analogs by total synthesisElectronic supplementary information (ESI) available: experimental details for the synthesis of 14 and 32. See http://www.rsc.org/suppdata/cc/b2/b209941a/
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Citations
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References
2002
Year
EngineeringHeterocyclicAlkene MetathesisNatural SciencesDiversity-oriented SynthesisSuzuki MacrocyclizationTotal SynthesisOrganic ChemistrySynthetic ChemistryChemistryEpothilone SeriesExperimental DetailsPharmacologyNozaki-kishi MacrocyclizationHeterocycle ChemistryNovel Epothilone AnalogsEnantioselective SynthesisBiomolecular Engineering
A total synthesis of Epothilone 490 and a synthesis of 11-hydroxy dEpoB utilizing a vinyl-boronate cross-metathesis followed by a Suzuki macrocyclization. A mild route to reach aldehydes from terminal olefins, anticipating Nozaki-Kishi macrocyclization is described.
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