N-Hydroxyphthalimide: a new photoredox catalyst for [4+1] radical cyclization of N-methylanilines with isocyanides

2016 ◽  
Vol 52 (70) ◽  
pp. 10621-10624 ◽  
Author(s):  
Arvind K. Yadav ◽  
Lal Dhar S. Yadav

A highly regioselective synthesis of 3-iminodihydroindoles using N-methylanilines and isocyanides at room temperature is described. The protocol utilizes N-hydroxyphthalimide as a new single electron transfer photoredox catalyst.

2016 ◽  
Vol 18 (19) ◽  
pp. 4900-4903 ◽  
Author(s):  
Joon Young Hwang ◽  
Jong Hwa Baek ◽  
Tae Il Shin ◽  
Jung Ha Shin ◽  
Jae Won Oh ◽  
...  

Synthesis ◽  
2019 ◽  
Vol 51 (13) ◽  
pp. 2697-2704 ◽  
Author(s):  
Quan-Zhe Li ◽  
Xun-Hui Wang ◽  
Si-Hua Hou ◽  
Yan-Yan Ma ◽  
Deng-Gao Zhao ◽  
...  

A simple and efficient protocol for para-selective C–H amination of 1-naphthylamide derivatives under silver catalysis is described. This reaction system could proceed without the help of directing group and a broad range of substrates were proved to be well tolerated. In addition, control experiments suggested that this reaction might not proceed via a single-electron-transfer process.


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...


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