Publication | Closed Access
A Route to the Thapsigargins from (<i>S</i>)‐Carvone Providing a Substrate‐Controlled Total Synthesis of Trilobolide, Nortrilobolide, and Thapsivillosin F
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Citations
15
References
2003
Year
Structural AnaloguesBioorganic ChemistrySubstrate-controlled Total SynthesisBiochemistryNatural SciencesSubstrate‐controlled Total SynthesisMolecular BiologyOrganic ChemistryStereoselective SynthesisThapsigargin FamilyHeterocycle ChemistryChemical BiologyPharmacologySynthetic ChemistryThapsivillosin FNatural Product Synthesis
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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