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- W2035531521 abstract "(S-Mandelic acid, (S)-lactic acid, and (S)-2-hydroxy-3-phenylpropionic acid react with thioacetic acid in the presence of the salt of diisopropyl azodicarboxylate and triphenylphosphine to give the α-(acetylthio)-substituted products. (S)-Mandelic acid reacts with predominant retention of configuration whereas (S)-lactic acid and (S)-2-hydroxy-3-phenylpropionic acid react predominantly with inversion. The involvement of α-lactone intermediates is very likely." @default.
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- W2035531521 date "1987-01-01" @default.
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- W2035531521 title "Evidence for α-lactone formation in the thioacetylation of some α-hydroxy acids with the aid of <i>Mitsunobu</i> -type reagent" @default.
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- W2035531521 doi "https://doi.org/10.1002/recl.19871061006" @default.
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