Phosphine-free Suzuki cross-coupling reaction: a mild and selective method for the carbon–carbon bond formation in aqueous tea extract

2014 ◽  
Vol 55 (40) ◽  
pp. 5539-5543 ◽  
Author(s):  
Limi Goswami ◽  
Pranjal Gogoi ◽  
Junali Gogoi ◽  
Ashwini Borah ◽  
Manash R. Das ◽  
...  
ChemInform ◽  
2012 ◽  
Vol 43 (33) ◽  
pp. no-no
Author(s):  
Yasunari Monguchi ◽  
Keita Sakai ◽  
Koichi Endo ◽  
Yuki Fujita ◽  
Masaru Niimura ◽  
...  

1995 ◽  
Vol 50 (3) ◽  
pp. 385-393 ◽  
Author(s):  
Yih-Ling Tzeng ◽  
Wen-Lung Cheng ◽  
Tien-Yau Luh

NiCl2(PPh3)2-catalyzed alkylative olefinations of trithioorthoesters and tetrathioorthocarbonates give the corresponding substituted alkenes. Aliphatic C - S bonds in these substrates can be activated in the nickel-catalyzed cross coupling reaction leading to carbon - carbon bond formation. This reaction can be considered as using trithioorthoesters and tetrathioorthocarbonate as R3C3+ and C4+ synthons.


ChemCatChem ◽  
2012 ◽  
Vol 4 (4) ◽  
pp. 546-558 ◽  
Author(s):  
Yasunari Monguchi ◽  
Keita Sakai ◽  
Koichi Endo ◽  
Yuki Fujita ◽  
Masaru Niimura ◽  
...  

2019 ◽  
Vol 10 (24) ◽  
pp. 6107-6112 ◽  
Author(s):  
Miku Oi ◽  
Ryo Takita ◽  
Junichiro Kanazawa ◽  
Atsuya Muranaka ◽  
Chao Wang ◽  
...  

A potent cross-coupling methodology that enables efficient carbon–carbon bond formation at sterically hindered sp2- and sp3-carbons has been developed.


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