The thermal peroxidation of cholesteryl acetate (CA) generates many compounds, most of which have been identified in previous studies. The trimethylsilyl (TMS) derivatives of the thermodegradation products of the single hydroperoxides of CA (7 alpha- and 7 beta-) gave GC-MS spectra that were almost identical to those of the thermal peroxidation of CA, except for four compounds that were only detected as TMS derivatives. These substances were identified by comparing their mass spectra and their GC retention time against those of the four synthesized isomers of the epoxy-hydroxy derivatives of CA. The presence of a considerable amount of epoxy-hydroxy derivates of CA, especially at low-temperature degradations, provides an explanation for the...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
The accurate analysis of trace component in complex biological matrices requires the use of reliable...
5-Hydroxy-1-oxo-5a-cholestan-3b-yl acetate (11) was prepared in 5 steps starting from (E)-3b-acetoxy...
The thermal peroxidation of cholesteryl acetate (CA) generates many compounds, most of which have be...
The thermal degradation products of the 7\u3b1- and 7\u3b2-cholesteryl 3\u3b2-acetate hydroperoxides...
The polar products separated by solid-phase extraction from the peroxidation mixture of cholesteryl ...
Gas chromatographic, high performance liquid chromatographic and GC-ion trap detector mass spectrome...
The thermal degradation of the two hydroperoxy isomers (7a- and 7b-hydroperoxides) of cholest-5-ene ...
A peroxidation mixture containing methyl 9- and 10-hydroperoxy-trans-octadecenoates (MOHP) was obtai...
Formation of cholesterol oxidation products (COPs) during dry heating of cholesterol films at 150\ub...
Gas chromatography - mass spectrometry offers a convenient method for the separation and identificat...
Oxidation of cholesterol (Ch) by a variety of reactive oxygen species gives rise mainly to hydropero...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
The accurate analysis of trace component in complex biological matrices requires the use of reliable...
5-Hydroxy-1-oxo-5a-cholestan-3b-yl acetate (11) was prepared in 5 steps starting from (E)-3b-acetoxy...
The thermal peroxidation of cholesteryl acetate (CA) generates many compounds, most of which have be...
The thermal degradation products of the 7\u3b1- and 7\u3b2-cholesteryl 3\u3b2-acetate hydroperoxides...
The polar products separated by solid-phase extraction from the peroxidation mixture of cholesteryl ...
Gas chromatographic, high performance liquid chromatographic and GC-ion trap detector mass spectrome...
The thermal degradation of the two hydroperoxy isomers (7a- and 7b-hydroperoxides) of cholest-5-ene ...
A peroxidation mixture containing methyl 9- and 10-hydroperoxy-trans-octadecenoates (MOHP) was obtai...
Formation of cholesterol oxidation products (COPs) during dry heating of cholesterol films at 150\ub...
Gas chromatography - mass spectrometry offers a convenient method for the separation and identificat...
Oxidation of cholesterol (Ch) by a variety of reactive oxygen species gives rise mainly to hydropero...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
International audienceGC-MS and GC-FTIR were complementarily applied to identify oxidation compounds...
The accurate analysis of trace component in complex biological matrices requires the use of reliable...
5-Hydroxy-1-oxo-5a-cholestan-3b-yl acetate (11) was prepared in 5 steps starting from (E)-3b-acetoxy...