Electron transfer free radical mechanism in the reactions of arenediazonium cations with grignard reagents

1982 ◽  
Vol 23 (52) ◽  
pp. 5475-5478
Author(s):  
P Singh
1953 ◽  
Vol 31 (12) ◽  
pp. 1211-1222 ◽  
Author(s):  
Jaspar J. Conn ◽  
Alfred Taurins

The ultraviolet absorption spectra of the low and high melting forms of β-aminocrotononitrile (I) provide evidence that both of them possess the same enamine structure. Since the existence of the polymorphic modifications of I must be excluded on the basis of the thermochemical behavior of I, the difference of the two modifications is capable of accounting for cis and trans isomerism, the low melting modification being the cis form, and the high melting modification being the trans form.In the reaction of I with aromatic Grignard reagents β-amino ketones of the type CH3—CO—CH==C(NH2)—R are formed as the main reaction products.The free radical mechanism of the formation of I is postulated.


2000 ◽  
Vol 127 (1) ◽  
pp. 61-72 ◽  
Author(s):  
Corwin Hansch ◽  
Susan C. McKarns ◽  
Carr J. Smith ◽  
David J. Doolittle

Author(s):  
Zhiying Fan ◽  
Zhifan Wang ◽  
Ruoyi Shi ◽  
Yuanhua Wang

Unlike C-N bond formation with classical dirhodium(II)-nitrenoids as the key intermediate, dirhodium(II)-catalyzed 1,2-and 1,3-diamination reactions are realized by a free radical mechanism. A mechanistic study revealed that the reactions undergo...


Sign in / Sign up

Export Citation Format

Share Document