Electron and chemical ionization mass spectrometry in stereochemical differentiation of some 1,3-amino alcohols
Author:
Publisher
Wiley
Subject
Spectroscopy,Instrumentation,Molecular Medicine,Biochemistry
Reference44 articles.
1. Spectrographie de masse en série du bornane—II: Amino-bornanols et dérivés
2. Electron impact and chemical ionization mass spectra of norbornane/ene di-exo and di-endo-fused 1,3-oxazin-2(1H)-ones and 1,3-oxazine-2(1H)-thiones
3. Differentiation of isomeric camphane-2,3-diols by NMR spectroscopy and chemical ionization mass spectrometry
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1. Electron ionization-induced fragmentation of bridgehead-substituted norbornan-2-ones derived from fenchone;International Journal of Mass Spectrometry;2013-01
2. Electron ionization mass spectral studies of bridgehead-substituted norbornan-2-ones: camphor derivatives;Rapid Communications in Mass Spectrometry;2011-01-07
3. Diastereomeric differentiation of two pairs of glycal derivatives by electrospray ionization tandem mass spectrometry;Rapid Communications in Mass Spectrometry;2010-08-24
4. Diastereomeric differentiation of norbornene amino acid peptides by electrospray ionization tandem mass spectrometry;Rapid Communications in Mass Spectrometry;2009-08-13
5. Electron ionisation mass spectral studies of bridgehead-fused Δ2-norbornanethiazolines;Rapid Communications in Mass Spectrometry;2009-03-30
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