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S-Thioacyldithiophosphates in the Synthesis of Thiohydroxamic Acids and O-Thioacylhydroxylamines
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2002
Year
BiosynthesisBioorganic ChemistryCarboxylic AcidsBiochemistryEngineeringHydroxy GroupBiocatalysisNatural SciencesOrganic ChemistryThiohydroxamic AcidsHigh YieldStereoselective SynthesisPharmacologySynthetic ChemistryEnantioselective SynthesisNatural Product Synthesis
S-Thioacyldithiophosphates proved to be excellent thioacylating agents. They are easily available from carboxylic acids. Due to their low reactivity towards oxygen nucleophiles and high reactivity towards nitrogen ones they found application in the synthesis of thiohydroxamic acids directly from hydroxylamines without protection on the hydroxy group. However, in cases of steric hindrance O-thioacyl hydroxylamines are formed and can be isolated with high yield.