Publication | Closed Access
A Concise Total Synthesis of <scp>dl</scp>-Histrionicotoxin
81
Citations
26
References
2006
Year
Medicinal ChemistryBiosynthesisBioorganic ChemistryTwo-directional Synthesis StrategyBiochemistryEngineeringSelective ZNatural SciencesToxinologyHeterocyclicOrganic ChemistryTwo-directional Cross-metathesisChemistryHeterocycle ChemistrySynthetic ChemistryBiomolecular EngineeringConcise Total Synthesis
The synthesis of (+/-)-histrionicotoxin has been achieved in just nine steps using a two-directional synthesis strategy. Key reactions include a two-directional cross-metathesis, a tandem oxime formation/Michael addition/1,4-prototopic shift/[3 + 2]-cycloaddition cascade, a selective Z,Z-bisenyne formation, and a one-pot N-O and bischloroacetylene reduction.
| Year | Citations | |
|---|---|---|
Page 1
Page 1