Key fragmentation patterns of aporphine alkaloids by electrospray ionization with multistage mass spectrometry

Rapid Communications in Mass Spectrometry

Volumn 18, Issue 5, 2004, Pages 523-528

  Stévigny, Caroline ^a   Jiwan, Jean Louis Habib ^a   Rozenberg, Raoul ^a   De Hoffmann, Edmond ^a   Quetin Leclercq, Joëlle ^a  

^a UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOIDS; ELECTRODEPOSITION; MASS SPECTROMETRY; METABOLITES;

AMINO GROUP; APORPHINE ALKALOIDS; AROMATIC RINGS; FRAGMENTATIONS PATTERN; MULTI-STAGE MASS SPECTROMETRY; POSITIVE MODE; RADICAL LOSS; SPECTRA'S;

ELECTROSPRAY IONIZATION;

ACTINODAPHNINE; APORPHINE DERIVATIVE; AROMATIC COMPOUND; BOLDINE; BULBOCAPNINE; CARBON MONOXIDE; CASSYTHINE; DICENTRINE; FORMALDEHYDE; GLAUCINE; HYDROXIDE; ISOCORYDINE; METHANOL; NEOLITSINE; NORNEOLITSINE; UNCLASSIFIED DRUG;

ARTICLE; DRUG IDENTIFICATION; DRUG STRUCTURE; ELECTROSPRAY; FRAGMENTATION REACTION; IONIZATION; MASS SPECTROMETRY; STRUCTURE ANALYSIS;

EID: 1542378880     PISSN: 09514198     EISSN: None     Source Type: Journal    
DOI: 10.1002/rcm.1343     Document Type: Article

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