Electron-induced ionization of undeuterated and deuterated benzoic acid isopropyl esters and nicotinic acid isopropyl esters: some implications for the mechanism of the McLafferty rearrangement
Gespeichert in:
| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2020
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| In: |
European journal of mass spectrometry
Year: 2019, Jahrgang: 26, Heft: 1, Pages: 3-24 |
| ISSN: | 1751-6838 |
| DOI: | 10.1177/1469066719857994 |
| Online-Zugang: | Resolving-System, Volltext: https://doi.org/10.1177/1469066719857994 Verlag: https://journals.sagepub.com/doi/full/10.1177/1469066719857994 
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| Verfasserangaben: | Joachim Opitz, A Stephen K Hashmi, Burkhard Miehlich and Michael Wölfle |
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| 245 | 1 | 0 | |a Electron-induced ionization of undeuterated and deuterated benzoic acid isopropyl esters and nicotinic acid isopropyl esters |b some implications for the mechanism of the McLafferty rearrangement |c Joachim Opitz, A Stephen K Hashmi, Burkhard Miehlich and Michael Wölfle |
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| 650 | 4 | |a concerted or stepwise reaction | |
| 650 | 4 | |a distonic ions | |
| 650 | 4 | |a enthalpies of formation | |
| 650 | 4 | |a McLafferty rearrangements | |
| 650 | 4 | |a single and double hydrogen transfer | |
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