Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of Amides via Site-Selective N–C Bond Cleavage by Cooperative Catalysis

ACS Catalysis ◽  
2016 ◽  
Vol 6 (11) ◽  
pp. 7335-7339 ◽  
Author(s):  
Guangrong Meng ◽  
Shicheng Shi ◽  
Michal Szostak
Keyword(s):  
Bond Cleavage ◽  
Cross Coupling ◽  
Cooperative Catalysis ◽  
Palladium Catalyzed ◽  
Site Selective

ChemInform Abstract: Palladium-Catalyzed C-P Cross-Coupling of Arylhydrazines with H-Phosphonates via C-N Bond Cleavage.

ChemInform ◽  
2015 ◽  
Vol 46 (13) ◽  
pp. no-no
Author(s):  
Wentao Xu ◽  
Gaobo Hu ◽  
Pengxiang Xu ◽  
Yuxing Gao ◽  
Yingwu Yin ◽  
...  
Keyword(s):  
Bond Cleavage ◽  
Cross Coupling ◽  
Palladium Catalyzed

scholarly journals Palladium catalyzed Suzuki cross-coupling of benzyltrimethylammonium salts via C–N bond cleavage

RSC Advances ◽  
2017 ◽  
Vol 7 (26) ◽  
pp. 15805-15808 ◽  
Author(s):  
Tao Wang ◽  
Shuwu Yang ◽  
Silin Xu ◽  
Chunyu Han ◽  
Ge Guo ◽  
...  
Keyword(s):  
Bond Cleavage ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Efficient Approach ◽  
Highly Efficient ◽  
Cross Coupling Reactions ◽  
Palladium Catalyzed ◽  
The Way

A Pd catalyzed Suzuki cross-coupling of a benzyltrimethylammonium salt is described. This reaction offers a highly efficient approach to diarylmethanes and also paves the way for the application of benzyltrimethylammonium salts in Pd catalyzed cross-coupling reactions.

Palladium-catalyzed Suzuki cross-couplings of N′-mesyl arylhydrazines via C–N bond cleavage

RSC Advances ◽  
2014 ◽  
Vol 4 (49) ◽  
pp. 25576-25579 ◽  
Author(s):  
He-Ping Zhou ◽  
Jin-Biao Liu ◽  
Jian-Jun Yuan ◽  
Yi-Yuan Peng
Keyword(s):  
Boronic Acid ◽  
Bond Cleavage ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Mild Conditions ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
High Yields ◽  
Aryl Boronic Acid ◽  
Biaryl Compounds

An efficient palladium-catalyzed Suzuki cross-coupling reaction of N′-mesyl arylhydrazine with aryl boronic acid is described, which affords the corresponding biaryl compounds in high yields. This transformation proceeds through C–N bond cleavage under mild conditions.

N-Acylsuccinimides: twist-controlled, acyl-transfer reagents in Suzuki–Miyaura cross-coupling by N–C amide bond activation

2017 ◽  
Vol 15 (42) ◽  
pp. 8867-8871 ◽  
Author(s):  
Yuki Osumi ◽  
Chengwei Liu ◽  
Michal Szostak
Keyword(s):  
Bond Activation ◽  
Bond Cleavage ◽  
Cross Coupling ◽  
Amide Bond ◽  
Acyl Transfer ◽  
Palladium Catalyzed

The palladium-catalyzed Suzuki–Miyaura cross-coupling of N-acylsuccinimides as versatile acyl-transfer reagents via selective amide N–C bond cleavage is reported.

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