ChemInform Abstract: One-Pot Tandem Synthesis of Furo[3,2-h]quinolines by a Sonogashira Cross-Coupling and Cyclization Reaction Supported by Basic Alumina under Microwave Irradiation.

ChemInform ◽  
2010 ◽  
Vol 41 (23) ◽  
pp. no-no
Author(s):  
Nirup B. Mondal ◽  
et al. et al.
Synthesis ◽  
2009 ◽  
Vol 2010 (03) ◽  
pp. 486-492 ◽  
Author(s):  
Nirup Mondal ◽  
Pritam Saha ◽  
Subhendu Naskar ◽  
Rupankar Paira ◽  
Shyamal Mondal ◽  
...  

Molecules ◽  
2013 ◽  
Vol 18 (11) ◽  
pp. 13860-13869 ◽  
Author(s):  
Leping Ye ◽  
Lin Yu ◽  
Lijun Zhu ◽  
Xiaodong Xia

ACS Omega ◽  
2018 ◽  
Vol 3 (4) ◽  
pp. 4534-4544 ◽  
Author(s):  
Jin Liu ◽  
Yu-Ling Wang ◽  
Ji-Hong Zhang ◽  
Jian-Shan Yang ◽  
Han-Chuan Mou ◽  
...  

2011 ◽  
Vol 66 (8) ◽  
pp. 833-836
Author(s):  
Zhiping Che ◽  
Hui Xu

An efficient one-pot synthesis of dibenzofurans, via SNAr reaction of aryl halides and ortho-bromophenols in the presence of anhydrous K2CO3 and subsequent ligand-free palladium-catalyzed intramolecular aryl-aryl cross-coupling cyclization under microwave irradiation, is described.


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.


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