Differences in the formation and fragmentation of sodium adduct ions between tertiarybutoxycarbonyl-protected prolylproline diastereomers in fast atom bombardment mass spectrometry

Citation
H. Tsunematsu et al., Differences in the formation and fragmentation of sodium adduct ions between tertiarybutoxycarbonyl-protected prolylproline diastereomers in fast atom bombardment mass spectrometry, CHEM PHARM, 47(7), 1999, pp. 1040-1043
Citations number
14
Categorie Soggetti
Chemistry & Analysis
Journal title
CHEMICAL & PHARMACEUTICAL BULLETIN
ISSN journal
00092363 → ACNP
Volume
47
Issue
7
Year of publication
1999
Pages
1040 - 1043
Database
ISI
SICI code
0009-2363(199907)47:7<1040:DITFAF>2.0.ZU;2-C
Abstract
The effect of Na+ ions on the fragmentation of tertiarybutoxycarbonyl (Boc) protected prolylproline (Pro-Pro) diastereomers, Boc-Pro-Pro and Boc-D-Pro -Pro, was studied in positive-ion fast atom bombardment (FAB) and tandem ma ss spectrometry. The formation of the [M+Na](+) ion for Boc-D-Pro-Pro was m ore predominant than that for Boc-Pro-Pro on the addition of sodium chlorid e in positive-ion FAB mass spectrometry, suggesting that Boc-D-Pro-Pro has a stronger Na+ ion affinity than Boc-Pro-Pro. In the collisional-activated decomposition mass spectra of the [M+Na](+) ions, the abundance of the [M+N a-C(CH3)(3)+H](+) ion, which is due to the loss of a tertiarybutyl group fr om the [M+Na](+) ion for Boc-D-Pro-Pro, was higher than that for Poe-pro-Pr o. These results indicate that the interaction of the Naf ion with Boc-Pro- Pro is different from that with Boc-D-Pro-Pro in the FAB condition, and the se diastereomers are distinguished by the addition of a Na+ ion in FAB and tandem mass spectrometry.