Electron impact and chemical ionization mass spectra of bis(methoxycarbonyl) [2.2](2,5)pyridinophanes. Formation of quinolizinium ions under electron impact
Author:
Publisher
Wiley
Subject
Spectroscopy,Instrumentation,Molecular Medicine,Biochemistry
Reference8 articles.
1. Bis(methoxycarbonyl)[2.2](2,5)pyridinophanes as nicotinamide coenzyme models
2. and Liebigs Ann. Chem., In press.
3. Macro rings. XXXVII. Multiple electrophilic substitution reactions of [2.2]paracyclophanes and interconversions of polysubstituted derivatives
4. Orientierungseffekte auf Charge‐Transfer‐Wechselwirkungen, VI. Die beiden intramolekularen Chinhydrone der [2.2]Paracyclophan‐Reihe
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1. Cyclization of diaza[6]helicenes to monoazacoronenes under electron impact;Tetrahedron Letters;1994-11
2. The behavior of stereoisomeric cyclohexane-1,2-, -1,3-, and -1,4-dicarboxylates under chemical ionization and collision induced dissociation. Conformational effects in gas-phase cations;Journal of the American Chemical Society;1993-08
3. Dithia[3.3 ]phanes. 4—mass spectrometry of some dithia[3.3]-naphthalenophanes1;Organic Mass Spectrometry;1991-07
4. Electron ionization and chemical ionization fragmentation ofo/p isomers of bisphenol-A with tandem mass spectrometry;Organic Mass Spectrometry;1988-04
5. Mass spectral studies of some [2.2]paracyclophanylethene derivatives;Organic Mass Spectrometry;1987-10
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