Substituent effects in charge exchange chemical ionization mass spectrometry

1986 ◽  
Vol 58 (11) ◽  
pp. 2121-2126 ◽  
Author(s):  
William J. Simonsick ◽  
Ronald A. Hites
1977 ◽  
Vol 32 (5) ◽  
pp. 573-580 ◽  
Author(s):  
C. C. Van de Sande ◽  
F. Van Gaever ◽  
P. Sandra ◽  
J. Monstrey

The helium charge exchange and the isobutane chemical ionization spectra of 4-methoxy cyclohexanecarboxylic acid ethyl esters (1c and 1t), 2,6-dimethyl-4-hydroxytetrahydropyranes (2c and 2t), 2,4,6-trimethyl-4-hydroxytetrahydropyranes (8c and 3t), and 2,7-dimethoxy-cis-decalins (4c and 4t) have been screened for correlations with the stereochemistry of these molecules. From these data it appears that chemical ionization is especially suited for configurational assignments in epimeric molecules.


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