Oxone®: A Convenient Reagent for the Oxidation of Acetals
M Curini, F Epifano, MC Marcotullio, O Rosati
Index: Curini, Massimo; Epifano, Francesco; Marcotullio, Maria Carla; Rosati, Ornelio Synlett, 1999 , # 6 p. 777 - 779
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Citation Number: 40
Abstract
Abstract: Symmetrical cyclic and acyclic acetals by oxidation with Oxone® gave the corresponding esters in good yield. Treatment of tetrahydropyranyl derivatives of alcohols with the same reagent resulted in oxidative regeneration of the alcohols. Key words: Oxone®, acetal oxidation, tetrahydropyranyl ether cleavage, glycol monoester formation
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