Angewandte Chemie International Edition · 2003 · 120 citations · 15 references
PharmacyChemistryPharmacologyDrug DiscoveryNatural Product BiosynthesisSynthetic Medicinal ChemistryOrganic SynthesisTarget-oriented SynthesisHeterocyclic Natural ProductsNatural Product SynthesisNatural Product Total SynthesisTotal Synthesis-derived Analogues
An entirely substrate-controlled total synthesis of three members of the thapsigargin family (e.g. trilobolide) is achieved starting from (S)-carvone. The synthesis is linear in nature but is achieved in high yield (>90 % per step). The route permits late-stage divergence, providing access to a range of natural products and structural analogues.
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