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- W2038888309 abstract "Acetoxyalkoxyacetic esters 1–8, prepared in two steps from methyl glyoxylate and unsaturated alcohols, cyclize under the influence of tin tetrachloride in dichloromethane to oxacyclic carboxylic esters 9–18 (Table). These ring closures proceed through the intermediacy of methoxycarbonyloxonium ions (C), most likely accompanied by cationic oxa-Cope rearrangements in some cases." @default.
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- W2038888309 title "Synthesis of oxacyclic carboxylic esters by way of methoxycarbonyloxonium ions; Evidence for a cationic oxa-cope rearrangement" @default.
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