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Profiling of structurally labile oxylipins in plants by in situ derivatization with pentafluorobenzyl hydroxylamine

MPG-Autoren
http://pubman.mpdl.mpg.de/cone/persons/resource/persons4168

Schulze,  B.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons4008

Lauchli,  R.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons4048

Mekem Sonwa,  M.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons4145

Schmidt,  Annika
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;
IMPRS on Ecological Interactions, MPI for Chemical Ecology, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons3812

Boland,  W.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

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Zitation

Schulze, B., Lauchli, R., Mekem Sonwa, M., Schmidt, A., & Boland, W. (2006). Profiling of structurally labile oxylipins in plants by in situ derivatization with pentafluorobenzyl hydroxylamine. Analytical Biochemistry, 348(2), 269-283. doi:10.1016/j.ab.2005.10.021.


Zitierlink: http://hdl.handle.net/11858/00-001M-0000-0012-A35A-3
Zusammenfassung
A GC-MS-based method for the simultaneous quantification of common oxylipins along with labile and highly reactive Compounds based on in situ derivatization with pentafluorobenzyl hydroxylamine to the corresponding O-2,3,4,5,6-pentafluorobenzyI oximes (