Catalyst-free amination of α-cyanoarylacetates enabled by single-electron transfer

2019 ◽  
Vol 6 (11) ◽  
pp. 1900-1904 ◽  
Author(s):  
Wei Zhang ◽  
Han-Liang Zheng ◽  
Yang Liu ◽  
Ao Yu ◽  
Chen Yang ◽  
...  

A radical benzylic amination of α-cyanoarylacetates without the assistance of any transition-metal catalysts or external photosensitizers was realized.

2020 ◽  
Author(s):  
Lei Chen ◽  
Shiyi Jin ◽  
Jian Gao ◽  
Tongtong Liu ◽  
Yuebo Shao ◽  
...  

An N-heterocyclic carbene and magnesium co-catalyzed three-component alkylacylation of alkenes with cycloketone oxime esters and aldehydes was presented. This method displayed good scope generality, providing a transition metal and photo-redox free pathway to access various multi-functionalized aliphatic keto-nitrile structures under mild reaction conditions. Moreover, this strategy is supposed to follow a radical relay mechanism via a single electron transfer (SET) event of Mg/oxime ester/Breslow intermediate ternary electron donating acceptor (EDA) complex.


SynOpen ◽  
2021 ◽  
Author(s):  
Addison M Duda ◽  
Michael T Giurini ◽  
Jason G Gillmore ◽  
Thomas F Guarr

Synthetic preparation of carbazoles can be challenging, requiring ring building strategies and/or precious metal catalysts. Presented herein is a method for preparation of carbazoles with the use of inexpensive and reliable hypervalent iodine chemistry. An oxidative single electron transfer (SET) event initiates cyclization for preparation of our trifluoromethyl carbazoles. This method has been shown to be useful for a variety of bis(trifluoromethyl)carbazole isomers that are of primary interest for use as battery materials.


ChemInform ◽  
2014 ◽  
Vol 45 (42) ◽  
pp. no-no
Author(s):  
Suresh Kumar Sythana ◽  
Santhosh Unni ◽  
Yogesh M. Kshirsagar ◽  
Pundlik R. Bhagat

2020 ◽  
Author(s):  
Lei Chen ◽  
Shiyi Jin ◽  
Jian Gao ◽  
Tongtong Liu ◽  
Yuebo Shao ◽  
...  

An N-heterocyclic carbene and magnesium co-catalyzed three-component alkylacylation of alkenes with cycloketone oxime esters and aldehydes was presented. This method displayed good scope generality, providing a transition metal and photo-redox free pathway to access various multi-functionalized aliphatic keto-nitrile structures under mild reaction conditions. Moreover, this strategy is supposed to follow a radical relay mechanism via a single electron transfer (SET) event of Mg/oxime ester/Breslow intermediate ternary electron donating acceptor (EDA) complex.


2019 ◽  
Vol 58 (17) ◽  
pp. 5697-5701 ◽  
Author(s):  
Jingjing Wu ◽  
Phillip S. Grant ◽  
Xiabing Li ◽  
Adam Noble ◽  
Varinder K. Aggarwal

2021 ◽  
Vol 23 (5) ◽  
pp. 1714-1719
Author(s):  
Linlin Zhang ◽  
Zhengfen Liu ◽  
Xun Tian ◽  
Yujin Zi ◽  
Shengzu Duan ◽  
...  

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