Abstract
In the presence of phosphovanadomolybdic acids, e.g., H6PV3Mo9O40, desulfurization–oxygenation of various kinds of structurally diverse secondary and tertiary thioamides proceeded efficiently using molecular oxygen as the terminal oxidant, affording the corresponding amides in moderate to excellent yields. In addition, 18O-labeled amides could readily be synthesized using H218O as the oxygen source.
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