Synlett 2006(20): 3548-3549  
DOI: 10.1055/s-2006-951565
SPOTLIGHT
© Georg Thieme Verlag Stuttgart · New York

Synthetic Applications of Oxone®

Wei He*
Department of Chemistry, School of Pharmacy, Fourth Military Medical University, Xi’an 710032, P. R. of China
e-Mail: hewei_chem@yahoo.com.cn;
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Publikationsdatum:
08. Dezember 2006 (online)

Introduction

Oxone® consists of 2KHSO5 . KHSO4 . K2SO4; its active component is potassium peroxymonosulfate (KHSO5), a powerful oxidizing agent in synthetic organic chemistry which has proved to be a versatile reagent for various organic transformations. Oxone® is commercially available and can be used immediately. Apart from its well-known applications as oxidizing agent in some transformations reviewed by Narsaiah, [1] it has found a number of other ­applications in synthetic chemistry in recent years, such as deprotection of functional groups, functional-group transformations, and cleavage of linker molecules from solid support. It has also shown wide potential in chiral ketone-catalysed asymmetric epoxidation of alkenes [2] leading to a variety of natural product skeletons, where its unique ­regioselective properties gave excellent results for the preparation of key intermediates.