CHARACTERIZATION OF STEREOISOMERIC ALPHA-METHYLENE-GAMMA-LACTONE FURANOSIDIC DERIVATIVES BY DIRECT CHEMICAL-IONIZATION MASS-SPECTROMETRY AND LIQUID SECONDARY-ION MASS-SPECTROMETRY WITH TANDEM MASS-SPECTROMETRY
C. Borges et al., CHARACTERIZATION OF STEREOISOMERIC ALPHA-METHYLENE-GAMMA-LACTONE FURANOSIDIC DERIVATIVES BY DIRECT CHEMICAL-IONIZATION MASS-SPECTROMETRY AND LIQUID SECONDARY-ION MASS-SPECTROMETRY WITH TANDEM MASS-SPECTROMETRY, Rapid communications in mass spectrometry, 10(7), 1996, pp. 757-766
Several furanosidic derivatives have been found to have biological act
ivity and have been used both as fungicides and plant growth regulator
s. In particular, those carbohydrate derivatives that contain the alph
a-methylene-gamma-lactone unit have interesting potential applications
, The present study deals with the mass spectrometric characterization
of furanosidic compounds having a alpha-methylene-gamma-lactone unit,
using different ionization techniques: chemical ionization mass spect
rometry and liquid secondary ion mass spectrometry together with metas
table ion analysis and high-energy collision-induced dissociation, The
objective of this study was to determine the influence on the respect
ive fragmentation patterns of structural differences present in the st
ereoisomers. Common fragmentation differences relate to the extent of
the loss of water which occurs together with the loss of acetone and t
o the formation of C7H7+ ions.