The behaviour of arylsulfonylmethyl sulfonates under conditions of electron-impact. The loss of CH2O
Author:
Publisher
Wiley
Subject
Spectroscopy,Instrumentation,Molecular Medicine,Biochemistry
Reference20 articles.
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1. Sulphonylium ions in the gas phase;Organic Mass Spectrometry;1989-07
2. Micellar effects on the reaction of (arylsulfonyl)alkyl arenesulfonates with hydroxide ion. 2. The absence of substrate orientational effects in a series of sulfonates of different hydrophobicities;The Journal of Organic Chemistry;1985-10
3. Micellar effects on the reaction of (arylsulfonyl)alkyl arenesulfonates with hydroxide ion. 1. Microenvironmental and substituent effects in the Stern layer of cationic micelles;The Journal of Organic Chemistry;1984-11
4. Chemical ionization and electron impact mass spectra of thiosulfinates, thiosulfonates and sulfinyl sulfones;Organic Mass Spectrometry;1982-03
5. Studies in mass spectrometry. IV—Fragmentation of aryltriflates. Substituent effects on [ArO]+ ion abundances: Looking for a best suited electron energy in the steady state approach. Experimental evidence for the ‘through bond’ stabilization of aryl cations bymeta electron donor Substituents;Organic Mass Spectrometry;1977-08
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