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- W2077110862 abstract "Abstract The oxidation of 8,2′-S-anhydroadenosine (1a) has been investigated. The major product from the oxidation of 1a using 1-chlorobenzotriazole was the R-sulfoxide. The oxidation of 3′,5′-di-O-acetyl-8,2′-S-anhydroadenosine (1b) gave predominately the S-sulfoxide. These sulfoxides were found to be very succeptible to nucleophilic attack at C-8." @default.
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- W2077110862 title "Preparation, Characterization and Reactivity of Diastereomeric Sulfoxides of 8,2′-S-Anhydroadenosine" @default.
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- W2077110862 doi "https://doi.org/10.1080/07328318308079407" @default.
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