β Scribed by Leonard E. Brady
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The fragmentation behaviour of 18 vicinally substituted aminonitropyridines was studied under electron impact conditions. The decomposition patterns were found to be strongly dependent on the position of substituents The formation of the am analogue of carbazole seems phenylamioopyridine.
The modes of fragmentation of perchlorylbenzene (C6H6C10s) and its perdeutero derivative under electron impact are reported and discussed. The occurrence of the [C,H,O]and [C,H,O]+ ions is accounted for in terms of a novel phenyl migration from chlorine to oxygen.
## Abstract Studies of both high and low resolution spectra, and of metastable decompositions occurring in both the first and second fieldβfree regions of the mass spectrometer have led to a postulated scheme for the fragmentation of acridine under electronβimpact. There is no specific loss of labe
OMS Letters Dear Sir ## Electron Impact Induced Fragmentations of 5-Hydroxy-1,2pentadiene As part of our investigations on the behaviour of o-functionalized allenes and acetylenes upon electron impact,' we have been interested in the fragmentation of the p-allenic alcohol 1. This letter deals ma