Volume 19, Issue 2
Isocyclic Compounds
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ChemInform Abstract: Oxidation of Sulfides to Sulfoxides by 1-Acetyl-v-triazolo(4,5-b)pyridine/Hydrogen Peroxide System.

I. TORRINI

I. TORRINI

Ist. Chim. Farm. Tossicol., Univ. La Sapienza, 00185 Roma, Italy

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M. P. PARADISI

M. P. PARADISI

Ist. Chim. Farm. Tossicol., Univ. La Sapienza, 00185 Roma, Italy

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G. P. ZECCHINI

G. P. ZECCHINI

Ist. Chim. Farm. Tossicol., Univ. La Sapienza, 00185 Roma, Italy

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F. AGROSI

F. AGROSI

Ist. Chim. Farm. Tossicol., Univ. La Sapienza, 00185 Roma, Italy

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First published: January 12, 1988

Abstract

The sulfides (I) are converted to the sulfoxides (II) using the triazolopyridine/hydrogen peroxide reagent system mentioned in the title.

ChemInform Abstract

The sulfides (I) are converted to the sulfoxides (II) using the triazolopyridine/hydrogen peroxide reagent system mentioned in the title. Prolonged reaction time causes partial formation of the corresponding sulfones. Thianthrene (Ih), for example, produces the monosulfoxide (IIh), together with the sulfone (III) and the bissulfoxides (IV). This method is also applied to penicillins. Further examples are given in the original paper.

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