Structure analysis of triacylglycerol positional isomers using atmospheric pressure chemical ionisation mass spectrometry

Tetrahedron Letters

Volumn 37, Issue 47, 1996, Pages 8593-8596

  Mottram, Hazel R ^a   Evershed, Richard P ^b  

^a UNIVERSITY OF BRISTOL   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

TRIACYLGLYCEROL;

ARTICLE; DRUG STRUCTURE; IN VITRO STUDY; MASS SPECTROMETRY; TECHNIQUE;

EID: 0030592767     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01964-8     Document Type: Article

References (16)

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10. 11. Covey, T. R.; Lee, E. D.; Bruins, A. P.; Henion, J. D. Anal. Chem. 1986, 58(14), 1451.
11. 12. Byrdwell, W. C.; Emken, E. A. Lipids 1995, 30(2), 173-175.
12. 13. Neff W. E.; Byrdwell W. C. J. Am. Oil Chem. Soc. 1995, 72(10), 1185-1191.
13. 14. Neff W. E.; Byrdwell W. C. J. Liq. Chromatogr. 1995 18(20), 4165-4181.
14. -1. Spectra obtained by scanning Q2 over the range m/z 200 to 1000, with scan cycle time of 2 seconds.
15. 16. The following abbreviations are used to represent fatty acids: My, myristic, tetradecanoic (14:0); P, palmitic, hexadecanoic (16:0); S, stearic, octadecanoic (18:0); O, oleic, cis-9-octadecenoic (18:1). TAG are represented by their constituent fatty acids.
16. 17. Mottram, H. R.; Evershed, R. P. Unpublished results. Tetrahedron Leiters. Vol. 37, No. 47, pp. 8597-8600, 1996