Stereoselective elimination of the hydroxyl group in the diastereoisomers of benzyloxycarbonyl-protatd γ-hydroxy-L-ornithine in fast atom bombardment mass spectrometry-Reference-Cited by-同舟云学术

Stereoselective elimination of the hydroxyl group in the diastereoisomers of benzyloxycarbonyl-protatd γ-hydroxy-L-ornithine in fast atom bombardment mass spectrometry

Published:1993-08 Issue:8 Volume:28 Page:921-922
ISSN:0030-493X
Container-title:Organic Mass Spectrometry
language:en
Short-container-title:Org. Mass Spectrom.

Author:

Tsunematsu Hideaki,Yamamoto Magobei,Isobe Ryuichi,Mizusaki Koichi,Makisumi Satoru

Publisher

Wiley

Subject

Spectroscopy,Instrumentation,Molecular Medicine,Biochemistry

Reference10 articles.

1. Role of matrix for enhancement of stereochemical effects in collision-activated dissociation (cad) spectra of mh+ from epimeric indole alkaloids

2. Chiral recognition of lithium-coordinated diols using tandem mass spectrometry

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4. Differentiation of diastereomeric aminotetralins by metastable ion spectra of 2-oxazolidinone derivatives upon electron-impact ionization

5. The isolation of γ-hydroxyarginine, as its lactone, from seeds of Vicia sativa, and the identification of γ-hydroxyornithine as a naturally occurring amino acid

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1. Mass spectral study of diastereomers on electron impact, III: 2- bromo-3-acetoxysuccinates and tartrate diacetates;European Journal of Mass Spectrometry;1997

2. Mass spectral study of diastereomers by electron impact;Rapid Communications in Mass Spectrometry;1995

3. Differentiation among the four diastereomers of benzyloxycarbonyl-protected γ-hydroxyornithine in negative-ion fast atom bombardment mass spectrometry;Organic Mass Spectrometry;1994-05