Copper-catalysed cross coupling reaction under microwave irradiation conditions

2000 ◽  
Vol 2000 (11) ◽  
pp. 536-537 ◽  
Author(s):  
Jin-Xian Wang ◽  
Zhanxiang Liu Yulai Hu ◽  
Bangguo Wei
2016 ◽  
Vol 1 (15) ◽  
pp. 4721-4725 ◽  
Author(s):  
Bhaskaran Savitha ◽  
Ayyiliath M. Sajith ◽  
Eeda Koti Reddy ◽  
C. S. Ananda Kumar ◽  
M. Syed Ali Padusha

2002 ◽  
Vol 32 (10) ◽  
pp. 1607-1614 ◽  
Author(s):  
Jin-Xian Wang ◽  
Zhanxiang Liu ◽  
Yulai Hu ◽  
Bangguo Wei ◽  
Lin Bai

2009 ◽  
Vol 11 (7) ◽  
pp. 931 ◽  
Author(s):  
Pritam Saha ◽  
Subhendu Naskar ◽  
Priyankar Paira ◽  
Abhijit Hazra ◽  
Krishnendu B. Sahu ◽  
...  

2017 ◽  
Vol 41 (12) ◽  
pp. 705-708 ◽  
Author(s):  
Wenpeng Mai ◽  
Mingxiu Lv ◽  
Xiaofeng Zhang ◽  
Kui Lu

An efficient protocol for one-pot deoxygenative and regioselective synthesis of 2-arylsulfonylquinolines has been developed via iron-catalysed cross-coupling reaction of quinoline N-oxides with sodium arylsulfinates in moderate to good yields under microwave irradiation. The reactions proceeded over a broad range of substrates with good regioselectivity and functional group tolerance.


Synthesis ◽  
2020 ◽  
Vol 52 (08) ◽  
pp. 1279-1286
Author(s):  
Kamal K. Rajbongshi ◽  
Srinivas Ambala ◽  
Thavendran Govender ◽  
Hendrik G. Kruger ◽  
Per I. Arvidsson ◽  
...  

An efficient catalyst-free radical cross-coupling reaction between aromatic aldehydes and sulfoximines was developed. The reaction took place in the presence of N-bromosuccinimide as the radical initiator under microwave irradiation to afford the corresponding acylated sulfoximines in moderate to excellent yields (27 examples). This protocol proved to be rapid, easy to handle, and applicable to a broad scope of substrates.


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