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Gas chromatography-mass spectrometry of the picolinyl ester derivatives of deuterated acetylenic fatty acids

✍ Scribed by M.S.F. Lie Ken Jie; Y.C. Choi

Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
398 KB
Volume
625
Category
Article
ISSN
1873-3778

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πŸ“œ SIMILAR VOLUMES

Mass spectra of the picolinyl ester deri
Mass spectra of the picolinyl ester derivatives of some conjugated diacetylenic fatty acids
✍ M.S.F. Lie Ken Jie; Y.K. Cheung; S.H. Chau; W.W. Christie; E.Y. Brechany πŸ“‚ Article πŸ“… 1992 πŸ› Elsevier Science 🌐 English βš– 239 KB

The electron impact (EI) mass spectral analysis of the picolinyl esters of nine positional isomers of conjugated diacetylenic fatty acids showed prominent M + and [M-l] + peaks. In all cases there was a regular series of ions 14 amu apart in the high molecular weight range until the triple bond syst

Mass spectral characterization of picoli
Mass spectral characterization of picolinyl and methyl ester derivatives of isomeric thia fatty acids
✍ W. W. Christie; E. Y. Brechany; M. S. F. Lie Ken Jie; O. Bakare πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 530 KB

Picoliiyl and methyl ester derivatives of all the isomeric thialaurates and thiastearates, together with some dithiastearates, have been characterized by gas chromatography/mass spectrometry. The picolinyl ester derivatives give simple electron impact mass spectra in which ions formed by cleavage at