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ChemInform Abstract: Dispiro-1,2,4,5-tetraoxanes via Ozonolysis of Cycloalkanone O-Methyl Oximes: A Comparison with the Peroxidation of Cycloalkanones in Acetonitrile—Sulfuric Acid Media.

✍ Scribed by Yuxiang Dong; Jonathan L. Vennerstrom


Publisher
John Wiley and Sons
Year
2010
Weight
30 KB
Volume
30
Category
Article
ISSN
0931-7597

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✦ Synopsis


Dispiro-1,2,4,5-tetraoxanes via Ozonolysis of Cycloalkanone O-Methyl Oximes: A Comparison with the Peroxidation of Cycloalkanones in Acetonitrile-Sulfuric Acid Media. -Ozonolysis of the O-methyl oximes (I) is found to yield dispiro-1,2,4,5-tetraoxanes (II), whereas acid-catalyzed peroxidation leads to the hexaoxonanes (III) in most cases.

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