The cleavage of a CC double bond after chemical ionization with NO+ A complex rearrangement process1
GJ Bukovits, H Budzikiewicz
Index: Bukovits, G. J.; Budzikiewicz, H. Organic Mass Spectrometry, 1984 , vol. 19, # 1 p. 23 - 26
Full Text: HTML
Citation Number: 6
Abstract
In an earlier publication2 we showed that alkenes under chemical ionization (CI) conditions react in a specific way with NO': Electrophilic attack on the rr system of the double bond leads to two isomeric molecular ions which give rise to two series of ions of the composition C,H2,N0 (ions a, a' and b' in Scheme 1) during the formation of which one hyd- rogen is transferred with high specificity from the hydrocarbon portion lost. In addition, an ion ... -1-+--J 0' b 2 b', (114) ...
Related Articles:
Syntheses of hydroxy ketones from lactones
[Cavicchioli, Silvia; Savoia, Diego; Trombini, Claudio; Umani-Ronchi, Achille Journal of Organic Chemistry, 1984 , vol. 49, # 7 p. 1246 - 1251]
Syntheses of hydroxy ketones from lactones
[Cavicchioli, Silvia; Savoia, Diego; Trombini, Claudio; Umani-Ronchi, Achille Journal of Organic Chemistry, 1984 , vol. 49, # 7 p. 1246 - 1251]
Syntheses of hydroxy ketones from lactones
[Cavicchioli, Silvia; Savoia, Diego; Trombini, Claudio; Umani-Ronchi, Achille Journal of Organic Chemistry, 1984 , vol. 49, # 7 p. 1246 - 1251]