0000000000855936

AUTHOR

J. C. Jallageas

showing 2 related works from this author

Structural „memory effects” influencing decompositions of glucose alkoxide anions produced from monoterpene glycoside isomers in tandem mass spectrom…

1989

Isomeric glycoconjugates have been distinguished using desorption negative-ion chemical ionization/tandem mass spectrometry (DNCI–MS/MS). The structure of the leaving terpene influences the orientation of consecutive decompositions during collisionally activated decomposition (CAD) of [M–H]− ions which pass through a glucose alkoxide intermediate ion. This apparent „memory effect” can be rationalized by considering the production of anion-induced dipole complexes.

chemistry.chemical_classificationChemical ionizationCollision-induced dissociation[SDV]Life Sciences [q-bio]Monoterpene010401 analytical chemistryOrganic ChemistryGlycoside010402 general chemistryTandem mass spectrometry01 natural sciencesMedicinal chemistry0104 chemical sciencesAnalytical ChemistryIon[SDV] Life Sciences [q-bio]chemistry.chemical_compoundchemistryDesorptionAlkoxideOrganic chemistryComputingMilieux_MISCELLANEOUSSpectroscopyRapid Communications in Mass Spectrometry
researchProduct

Evidence and characterization of glycosidically bound volatile components in fruits

1988

International audience

0106 biological sciences[SDV] Life Sciences [q-bio]Chemistry[SDV]Life Sciences [q-bio]010608 biotechnologyOrganic chemistry01 natural sciencesComputingMilieux_MISCELLANEOUS010606 plant biology & botanyCharacterization (materials science)
researchProduct