Reactions of excited molecules. II. Reactions of phenylhydrazones on electron impact

1968 ◽  
Vol 21 (3) ◽  
pp. 761 ◽  
Author(s):  
WD Crow ◽  
JL Occolowitz ◽  
RK Solly

Electron impact data are presented for the phenylhydrazones of a series of aromatic ketones C6H5-CO-R (R = H, CH3, CD3, C2H5, C6H6), and are discussed in comparison with the results of thermal excitation. Whereas pyrolysis resulted in extensive four-centre migration of R to nitrogen, followed by (or synchronous with) cleavage of the N-X bond, the electron-impact breakdown is largely dominated by N-N bond cleavage. A semi-quantitative assessment is made of the rearrangements which do occur, and the stereochemistry of these and related reactions is discussed.

2001 ◽  
Vol 77 (2) ◽  
pp. 161-213 ◽  
Author(s):  
R. CELIBERTO ◽  
R.K. JANEV ◽  
A. LARICCHIUTA ◽  
M. CAPITELLI ◽  
J.M. WADEHRA ◽  
...  

2014 ◽  
Vol 543 (4) ◽  
pp. 199-244 ◽  
Author(s):  
Jung-Sik Yoon ◽  
Mi-Young Song ◽  
Deuk-Chul Kwon ◽  
Heechol Choi ◽  
Chang-Geun Kim ◽  
...  

2003 ◽  
Vol 125 (7) ◽  
pp. 1698-1699 ◽  
Author(s):  
Fumitoshi Kakiuchi ◽  
Shintaro Kan ◽  
Kimitaka Igi ◽  
Naoto Chatani ◽  
Shinji Murai

1969 ◽  
Vol 22 (6) ◽  
pp. 1219 ◽  
Author(s):  
JH Bowie ◽  
PJ Hoffmann

The mass spectra of anils with ortho-alkoxyl substituents in the aromatic ring derived from the aldehyde contain pronounced peaks prod- uced by C=N bond cleavage accompanied by one and/or two hydrogen transfers to the nitrogen-containing fragment. Deuterium-labelling studies show that the hydrogen atoms involved are those attached to the α-carbon (α to oxygen) of the alkoxyl group. The extent of the hydrogen rearrangements may be altered by the addition of further substituents to the aromatic rings.


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