Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Differences in the Formation and Fragmentation of Sodium Adduct Ions between Tertiarybutoxycarbonyl-Protected Prolyproline Diastereomers in Fast Atom Bombardment Mass Spectrometry
Hideaki TSUNEMATSU, Ryuichi ISOBE, Hiroshi HANAZONO, Yasuko SOEDA, Masanori INAGAKI, Naofumi ITO, Ryuichi HIGUCHI, Magobei YAMAMOTO
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1999 Volume 47 Issue 7 Pages 1040-1043

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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 mass spectrometry. The formaiton of the [M+Na]+ ion for Boc-D-Pro-Pro was more predominant than that for Boc-Pro-Pro on the addition of sodium chloride 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+Na-C(CH3)3+H]+ ion, which is due to the loss of a tertiarybutyl group from the [M+Na]+ ion for Boc-D-Pro-Pro, was higher than that for Bos-Pro-Pro. These results indicate that the interaction of the Na+ ion with Boc-Pro-Pro is different from that with Boc-D-Pro-Pro in the FAB condition, and these diastereomers are distinguished by the addition of a Na+ ion in FAB and tandem mass spectrometry.
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© The Pharmaceutical Society of Japan
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