Palladium-catalyzed Mizoroki–Heck-type reactions of [Ph2SRfn][OTf] with alkenes at room temperature

2016 ◽  
Vol 52 (80) ◽  
pp. 11893-11896 ◽  
Author(s):  
Shi-Meng Wang ◽  
Hai-Xia Song ◽  
Xiao-Yan Wang ◽  
Nan Liu ◽  
Hua-Li Qin ◽  
...  

The first Pd-catalyzed Mizoroki–Heck-type cross-coupling of phenylsulfonium salts with alkenes was disclosed at room temperature.

2010 ◽  
Vol 12 (19) ◽  
pp. 4388-4391 ◽  
Author(s):  
Jonathan T. Reeves ◽  
Daniel R. Fandrick ◽  
Zhulin Tan ◽  
Jinhua J. Song ◽  
Heewon Lee ◽  
...  

Molecules ◽  
2018 ◽  
Vol 23 (10) ◽  
pp. 2412 ◽  
Author(s):  
Weijia Shi ◽  
Gang Zou

A highly efficient acylative cross-coupling of trialkylboranes with activated amides has been effected at room temperature to give the corresponding alkyl ketones in good to excellent yields by using 1,3-bis(2,6-diisopropyl)phenylimidazolylidene and 3-chloropyridine co-supported palladium chloride, the PEPPSI catalyst, in the presence of K2CO3 in methyl tert-butyl ether. The scope and limitations of the protocol were investigated, showing good tolerance of acyl, cyano, and ester functional groups in the amide counterpart while halo group competed via the classical Suzuki coupling. The trialkylboranes generated in situ by hydroboration of olefins with BH3 or 9-BBN performed similarly to those separately prepared, making this protocol more practical.


ChemInform ◽  
2011 ◽  
Vol 42 (7) ◽  
pp. no-no
Author(s):  
Jonathan T. Reeves ◽  
Daniel R. Fandrick ◽  
Zhulin Tan ◽  
Jinhua J. Song ◽  
Heewon Lee ◽  
...  

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