One-Pot Synthetic Procedure for 2,2′-Disubstituted Biaryls via the Suzuki Coupling Reaction of Aryl Triflates in a Biphasic Solvent System.

ChemInform ◽  
2007 ◽  
Vol 38 (17) ◽  
Author(s):  
Masanori Miura ◽  
Takanori Koike ◽  
Tsukasa Ishihara ◽  
Fukushi Hirayama ◽  
Shuichi Sakamoto ◽  
...  
2006 ◽  
Vol 36 (24) ◽  
pp. 3809-3820 ◽  
Author(s):  
Masanori Miura ◽  
Takanori Koike ◽  
Tsukasa Ishihara ◽  
Fukushi Hirayama ◽  
Shuichi Sakamoto ◽  
...  

2015 ◽  
Vol 56 (33) ◽  
pp. 4744-4748 ◽  
Author(s):  
Eethamukkala Ubba ◽  
Y. Suneel Kumar ◽  
C. Dasaradhan ◽  
Fazlur-Rahman Nawaz Khan ◽  
Euh Duck Jeong ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (47) ◽  
pp. no-no
Author(s):  
Eethamukkala Ubba ◽  
Y. Suneel Kumar ◽  
C. Dasaradhan ◽  
Fazlur-Rahman Nawaz Khan ◽  
Euh Duck Jeong ◽  
...  

2014 ◽  
Vol 16 (17) ◽  
pp. 4558-4561 ◽  
Author(s):  
Yongda Zhang ◽  
Bruce Z. Lu ◽  
Guisheng Li ◽  
Sonia Rodriguez ◽  
Jonathan Tan ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 439
Author(s):  
Ana Dolšak ◽  
Kristjan Mrgole ◽  
Matej Sova

Suzuki coupling reaction has been often used for the preparation of a diverse set of substituted pyrimidines. In this study, the Suzuki coupling of 2,4-dichloropyrimidines with aryl and heteroaryl boronic acids was investigated. A thorough screening of reaction conditions and the use of microwave irradiation led to a very efficient and straightforward synthetic procedure providing C4-substituted pyrimidines in good to excellent yields. Short reaction time (15 min) and extremely low catalyst loading (0.5 mol%) are the main advantages of our tetrakis(triphenylphosphine)palladium(0) catalyzed microwave-assisted procedure, which could be used for quick and low-cost regioselective preparation of substituted pyrimidine rings.


2021 ◽  
Vol 6 (18) ◽  
pp. 4511-4514
Author(s):  
Daniela R. P. Loureiro ◽  
José X. Soares ◽  
Ana Maia ◽  
André M. N. Silva ◽  
Maria Rangel ◽  
...  

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