MnCl 2 ‐Mediated Carbonylative Sonogashira Coupling of Aryl Iodides and Aromatic Terminal Alkynes by Using CO

2019 ◽  
Vol 4 (39) ◽  
pp. 11553-11556
Author(s):  
Parvathi K. Lakshmi ◽  
Sarma V. Markandeya ◽  
Chidara Sridhar ◽  
Raghu Babu K
RSC Advances ◽  
2017 ◽  
Vol 7 (51) ◽  
pp. 31850-31857 ◽  
Author(s):  
Yan Wang ◽  
Xiaolong Yang ◽  
Jianqiang Yu

Pd nanoparticles immobilized on polysalen based on polyacylamide was synthesized and used for carbonylative Sonogashira coupling of aryl iodides with terminal alkynes to produce α,β-alkynyl ketones in aqueous media.


2009 ◽  
Vol 23 (2) ◽  
pp. 75-77 ◽  
Author(s):  
Jin Tao Guan ◽  
Guang-Ao Yu ◽  
Lei Chen ◽  
Tan Qing Weng ◽  
Jing Jing Yuan ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 41 (34) ◽  
pp. no-no
Author(s):  
Dinesh N. Sawant ◽  
Pawan J. Tambade ◽  
Yogesh S. Wagh ◽  
Bhalchandra M. Bhanage

2005 ◽  
Vol 83 (6-7) ◽  
pp. 711-715 ◽  
Author(s):  
Takahide Fukuyama ◽  
Ryo Yamaura ◽  
Ilhyong Ryu

A carbonylative three-component coupling reaction of aryl iodides with terminal alkynes catalyzed by PdCl2(PPh3)2 was carried out using an ionic liquid, [bmim]PF6, as the reaction medium, which resulted in good yields of α,β-acetylenic ketones. The low-viscosity ionic liquid, [bmim]NTf2, was not suitable for this reaction, since the background Sonogashira coupling reaction, a competing reaction, also proceeded.Key words: carbonylation, palladium, three-component coupling, ionic liquid, α,β-acetylenic ketones.


2010 ◽  
Vol 51 (20) ◽  
pp. 2758-2761 ◽  
Author(s):  
Dinesh N. Sawant ◽  
Pawan J. Tambade ◽  
Yogesh S. Wagh ◽  
Bhalchandra M. Bhanage

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