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Mass spectrometric studies on a β-ketosulfone

✍ Scribed by Dov Diller; Felix Bergmann


Publisher
John Wiley and Sons
Year
1977
Tongue
English
Weight
203 KB
Volume
12
Category
Article
ISSN
1076-5174

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✦ Synopsis


Abstract

The fragmentation of the β‐ketosulfone‐γ‐methylsulfonyl‐γ‐benzoylbutyronitrile under electron bombardment follows a number of different pathways: formation of the benzoyl ion (Major path); remova of acrylonitrile; liberation of the methylsulfonyl radical or of methylsulfonic acid; and finally elimination of a methylenecyano radical. The fragments observed can be explained by these five degradation paths. The reactions are compared with the photochemical cleavage of this β‐ketosulfone in benzene solution.


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