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- W2321124024 abstract "Starting from alkyl halides or Michael acceptors, thioacetates were prepared in situ and further treated with t-BuOCl, affording the corresponding sulfonyl chlorides which were trapped with nucleophiles such as water, alcohol, or amines. The three steps can be achieved in a one-pot procedure. Oxidative deprotection also proved to be efficient with S-trityl and S-tert-butyl groups, making it a convenient route toward cysteic acid derivatives." @default.
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- W2321124024 date "2013-04-19" @default.
- W2321124024 modified "2023-10-04" @default.
- W2321124024 title "Synthesis of Sulfonic Acid Derivatives by Oxidative Deprotection of Thiols Using <i>tert</i>-Butyl Hypochlorite" @default.
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- W2321124024 doi "https://doi.org/10.1021/ol400865b" @default.
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