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
Author:
Publisher
Wiley
Subject
Spectroscopy,Instrumentation,Molecular Medicine,Biochemistry
Reference14 articles.
1. Mass Spectrometry of Steroids, Wiley, New York (1976).
2. A stereochemical bridge between mass spectrometry and free radical chemistry
3. in Topics in Stereochemistry, vol. 9, pp. 35-110, edited by and Wiley-lnterscience, New York (1976).
4. Translational energy release and stereochemistry of steroids. VIII-The mechanism of the elimination of water from metastable ions in epimeric 3-hydroxy steroids of the 5α-series
5. Translational energy release and stereochemistry of steroids. IX-The mechanism of the elimination of water from metastable ions in epimeric 3-hydroxy steroids of the 5β-series
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3. Profiling 19-norsteroids. I—tandem mass spectrometric characterization of the heptafluorobutyryl ester and pentafluorobenzyloxime heptafluorobutyryl ester derivatives of 19-nortestosterone using collisionally activated dissociation;Journal of Mass Spectrometry;1995-03
4. 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
5. Translational energy release and stereochemistry of steroids. 14. Epimeric dihydroxy steroids of the androstane series;Rapid Communications in Mass Spectrometry;1989-10
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