Single-Electron-Transfer-Initiated Sequential Direct Arylation Reaction of Pyrrole with Aryl Diazonium Salts

2019 ◽  
Vol 8 (3) ◽  
pp. 324-327 ◽  
Author(s):  
Eiji Yamaguchi ◽  
Yayoi Kashima ◽  
Akichika Itoh
Synlett ◽  
2019 ◽  
Vol 30 (08) ◽  
pp. 875-884 ◽  
Author(s):  
Evi Habraken ◽  
Andrew Jupp ◽  
J. Slootweg

Aryldiazonium salts are widely used in many organic transformations with displacement of N2 or through addition to the terminal nitrogen. Such aryldiazonium salts can be viewed as N-based Lewis acids that can react with Lewis bases to synthesize a wide variety of azo compounds. Additionally, diazonium salts are known to undergo single-electron transfer and release N2, forming an aryl radical, which results in different reactivity. Herein, we provide a concise overview of the reactivity of aryldiazonium salts undergoing classical donor-acceptor reactivity or single-electron transfer.


Author(s):  
Sundarababu Baskaran ◽  
Kirana D V ◽  
Kanak Kanti Das

A one-pot catalytic method has been developed for the stereoselective synthesis of cyclopropane-fused cyclic amidines using CuBr2/K2S2O8 as an efficient single electron transfer (SET) oxidative system. The generality of this...


1984 ◽  
Vol 25 (45) ◽  
pp. 5107-5110 ◽  
Author(s):  
E.C. Ashby ◽  
Dong-Hak Bae ◽  
Won-Suh Park ◽  
Robert N. Depriest ◽  
Wei-Yang Su

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