Translational energy release and stereochemistry of steroids. X. The Effect of the 5,6-double bond on the elimination of angular methyls and water from metastable molecular ions of epimeric steroid alcohols
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference8 articles.
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4. Translational energy release and stereochemistry of steroids. VII—the loss of angular methyl groups after the dehydration of molecular ions of cholesterol and related C(5)-unsaturated 3β-hydroxy steroids
5. Electron impact induced fragmentation of cholesterol and related C-5 unsaturated steroids
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1. Stochastic dynamic mass spectrometric quantification of steroids in mixture — Part II;Steroids;2020-12
2. Translational energy release and stereochemistry of steroids 15. Reaction conformations of metastable molecular ions in stereoisomers of 3-hydroxy steroids;Rapid Communications in Mass Spectrometry;1990-02
3. Translational energy release and stereochemistry of steroids. 14. Epimeric dihydroxy steroids of the androstane series;Rapid Communications in Mass Spectrometry;1989-10
4. Mass spectrometry of metastable ions and stereochemistry of steroids;International Journal of Mass Spectrometry and Ion Processes;1988-12
5. Translational energy release and stereochemistry of steroids. XI—Determination of the configuration of α,β-unsaturated 3-keto steroid alcohols with the hydroxyl group in rings C and D;Organic Mass Spectrometry;1988-07
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