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The Preferred Mode of Cycloreversion of Some 1,3,4-substituted Azetidin-2-ones Upon Electron-impact
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Document type | Article de périodique (Journal article) – Article de recherche |
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Publication date | 1989 |
Language | Anglais |
Journal information | "Organic Mass Spectrometry" - Vol. 24, no. 1, p. 1-7 (1989) |
Peer reviewed | yes |
Publisher | John Wiley & Sons Ltd (W Sussex) |
issn | 0030-493X |
Publication status | Publié |
Affiliation | UCL |
Links |
- Bose, Tetrahedron, 23, 957 (1967)
- Singer, J. Am. Chem. Soc., 89, 941 (1967)
- Chapman, J. Am. Chem. Soc., 90, 2333 (1968)
- Sterk, Monatsh. Chem., 103, 615 (1972)
- Fischer, Chem. Ber., 101, 2669 (1968)
- and Bull. Soc. Chim. France 2297 (1967).
- Jackson, Org. Mass Spectrom., 1, 857 (1968)
- Bird, J. Chem. Soc., Perkin Trans., 1, 2664 (1973)
- PhD thesis, Louvain la Neuve (1976), to be published.
- Schwarz, Org. Mass Spectrom., 15, 491 (1980)
- and 12th Annual Conference on Mass Spectrometry, p. 150, Montreal (1964).
Bibliographic reference | Auriel, M. ; de Hoffmann, Edmond ; Scheers, P. ; Deffense, E.. The Preferred Mode of Cycloreversion of Some 1,3,4-substituted Azetidin-2-ones Upon Electron-impact. In: Organic Mass Spectrometry, Vol. 24, no. 1, p. 1-7 (1989) |
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Permanent URL | http://hdl.handle.net/2078.1/52672 |