Synthesis of antitrypanosomal 1,2-dioxane derivatives based on a natural product scaffold
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Labaied, Mehdi
Ngoc, Pham
Jenkins, Ian D
Stuart, Kenneth
Quinn, Ronald J
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Abstract
A short practical synthesis of a new natural product based scaffold (6), based on antitrypanosomal and antimalarial compounds isolated from different Plakortis species is described. The scaffold contains a peroxide unit that is surprisingly stable to chemical manipulation elsewhere in the molecule, enabling it to be elaborated into a small library of derivatives. It is stable to ozonolysis, reductive work-up with dimethylsulfide and the Wittig reaction with stabilized phosphorus ylides. The scaffold along with its Wittig analogues has displayed low to sub-micro molar (0.2-3.3 lM) antitrypanosomal activity.
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Bioorganic & Medicinal Chemistry Letters
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21
Issue
16
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Medicinal and biomolecular chemistry
Biologically active molecules
Medicinal and biomolecular chemistry not elsewhere classified
Organic chemistry
Organic chemical synthesis
Pharmacology and pharmaceutical sciences