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Several authors have reported on the different bioactivities of methyl jasmonate (MeJA) stereoisomers. However, no simple, precise and cheap method for separating and identifying them using reversed-phase high performance liquid chromatography (RP-HPLC) has been developed.

Separating and Identifying the Four Stereoisomers of Methyl Jasmonate by RP-HPLC and using Cyclodextrins in a Novel Way

Matencio Duran, Adrian
First
;
2017-01-01

Abstract

Several authors have reported on the different bioactivities of methyl jasmonate (MeJA) stereoisomers. However, no simple, precise and cheap method for separating and identifying them using reversed-phase high performance liquid chromatography (RP-HPLC) has been developed.
2017
PHYTOCHEMICAL ANALYSIS
28
3
151
158
RP-HPLC; cyclodextrin; docking; enantioseparation; methyl jasmonate; Acetates; Chromatography, High Pressure Liquid; Chromatography, Reverse-Phase; Cyclodextrins; Cyclopentanes; Hydrogen-Ion Concentration; Molecular Docking Simulation; Oxylipins; Reproducibility of Results; Stereoisomerism; Temperature; beta-Cyclodextrins
Matencio Duran, Adrian; Bermejo-Gimeno, Mario J; García-Carmona, Francisco; López-Nicolás, José Manuel
03A-Articolo su Rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1869059
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