Stepwise retro 1,3-dipolar cycloaddition induced by electron. Impact on 3,5-diphenyl-1,2,4-oxadiazole

Stepwise retro 1,3-dipolar cycloaddition induced by electron. Impact on 3,5-diphenyl-1,2,4-oxadiazole

The retro 1,3‐dipolar cycloaddition induced by electron impact on 3,5‐diphenyl‐1,2,4‐oxadiazole is interpreted as a two‐step process on the basis of the energetics and kinetics of the fragments [C7H5NO]+., [C6H5CN]+. and [C6H5CO]+.

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Veröffentlicht in:Organic Mass Spectrometry 1976-02, Vol.11 (2), p.217-218
Hauptverfasser: Selva, Antonio, Traldi, Pietro, Zerilli, Luigi F., Gallo, Gian Gualberto
Format: Artikel
Sprache:eng
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Zusammenfassung:The retro 1,3‐dipolar cycloaddition induced by electron impact on 3,5‐diphenyl‐1,2,4‐oxadiazole is interpreted as a two‐step process on the basis of the energetics and kinetics of the fragments [C7H5NO]+., [C6H5CN]+. and [C6H5CO]+.
ISSN:0030-493X
1096-9888
DOI:10.1002/oms.1210110219