Preferential alkali metal adduct formation by cis geometrical isomers of dicaffeoylquinic acids allows for efficient discrimination from their trans isomers during ultra-high-performance liquid chromatography/quadrupole time-of-flight mass spectrometry

Rapid Communications in Mass Spectrometry

Volumn 30, Issue 8, 2016, Pages 1011-1018

  Makola, Mpho M ^a   Steenkamp, Paul A ^a,b   Dubery, Ian A ^a   Kabanda, Mwadham M ^c   Madala, Ntakadzeni E ^a  

^a UNIVERSITY OF JOHANNESBURG   (South Africa)

^b DSI CSIR Nanotechnology Innovation Centre   (South Africa)

^c NORTH WEST UNIVERSITY   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

GEOMETRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ISOMERS; MASS SPECTROMETRY; PLANT EXTRACTS; STEREOCHEMISTRY;

ACID DERIVATIVE; ADDUCT FORMATION; CAFFEOYLQUINIC ACIDS; CONE VOLTAGE; FRAGMENTATIONS PATTERN; GEOMETRICAL ISOMERS; LIQUID CHROMATOGRAPHY-QUADRUPOLE TIME-OF-FLIGHT MASS SPECTROMETRIES; LIQUID CHROMATOGRAPHY/QUADRUPOLE-TIME OF FLIGHT MASS SPECTROMETRIES; STRUCTURAL DIVERSITY; ULTRA-HIGH PERFORMANCE LIQUID CHROMATOGRAPHIES;

MOLECULES;

ALKALI METAL; CAFFEOYLQUINIC ACID; QUINIC ACID;

ANALOGS AND DERIVATIVES; CHEMISTRY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ISOMERISM; MASS SPECTROMETRY; PROCEDURES;

CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ISOMERISM; MASS SPECTROMETRY; METALS, ALKALI; QUINIC ACID;

EID: 84961807051     PISSN: 09514198     EISSN: 10970231     Source Type: Journal    
DOI: 10.1002/rcm.7526     Document Type: Article

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