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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 30, 2000 - Issue 17
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Original Articles

Bis(1-Benzyl-3,5,7-Triaza-1-Azoniatricyclo[3.3.1.13,7] Decane) Peroxodisulfate: A Mild and Efficient Oxidation of Organic Compounds Under Anhydrous and Aprotic Conditions

, &
Pages 3127-3131 | Accepted 01 Nov 1999, Published online: 04 Dec 2007
 

Abstract

Bis (1-benzyl-3, 5, 7-triaza-1-azoniatricyclo[3.3.1.13,7] decane) perox-odisulfate was readily prepared as an white solid from commercically available hexam-ethylenetetramine and potassium peroxodisulfate. This reagent could be used as a stable, mild and efficient oxidizer to produce the corresponding carbonyl compounds from hydroxyl compounds or hydrazones or oximes and disulfides from thiols under anhydrous and aprotic conditions. The yields were almost quantitative, and the reaction time was very short.

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