Premium
Chemical ionization and high resolution electron impact mass spectra of 1,6‐anhydro‐3,4‐ O ‐isopropylidene‐β‐ D ‐talopyranose
Author(s) -
Horton Derek,
Jewell Jon S.,
Just Ernst K.,
Wander Joseph D.,
Foltz Rodger L.
Publication year - 1974
Publication title -
biomedical mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0306-042X
DOI - 10.1002/bms.1200010212
Subject(s) - chemistry , electron ionization , isobutane , mass spectrum , deuterium , fragmentation (computing) , chemical ionization , ion , ionization , spectral line , hydrogen , mass spectrometry , analytical chemistry (journal) , high resolution , atomic physics , organic chemistry , physics , operating system , remote sensing , chromatography , astronomy , computer science , geology , catalysis
The high resolution, electron impact mass spectrum of 1,6‐anhydro‐3,4‐ O ‐isopropylidene‐β‐ D ‐talopyranose, together with those of its derivatives having specific deuterium substitution at C‐2, at C‐3, at C‐2 and C‐3, and in the isopropylidene group, is considered in detail and compared with the ammonia and isobutane mediated chemical ionization spectra of these five compounds. From the elemental compositions of the fragment ions and mass number shifts upon deuterium incorporation, the origin of the hydrogen atoms in each of the fragments is traced, and a detailed scheme of the main fragmentation. pathways is presented.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom