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The fragmentation mechanism under electron impact of N-trifluoromethylsulfonyl derivatives of arenesulfonyl, imidoyl and di-imidoyl halides and amides

✍ Scribed by I.G. Krajnikova; L.M. Yagupolskii; R.Yu. Garlyauskaite


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
424 KB
Volume
71
Category
Article
ISSN
0022-1139

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## Abstract A study has been made of the fragmentation upon electron impact of thieno(2,3‐__b__)quinoline and sixteen of its derivatives containing methoxy, methylenedioxy, chloro, bromo, iodo, nitro and methyl substituents. Besides these, the fragmentation patterns of some __S__‐oxides, and __S,S_