ChemInform Abstract: Suzuki Reaction of Bromoallenes with Arylboronic Acids Using an Air-Stable Palladium Complex Pd(Ph2PCH2CO2)2 as a Precatalyst.

ChemInform ◽  
2010 ◽  
Vol 41 (40) ◽  
pp. no-no
Author(s):  
Xin Du ◽  
Xiu Juan Feng ◽  
Ying Liu ◽  
Ren He ◽  
Ming Bao
2004 ◽  
Vol 82 (2) ◽  
pp. 206-214 ◽  
Author(s):  
Richard W Friesen ◽  
Laird A Trimble

4,7-Dichloroquinoline (1a) and 7-chloro-4-iodoquinoline (1b) undergo Suzuki cross-coupling reactions with arylboronic acids catalyzed by phosphine-free palladium acetate in boiling water. Using phenylboronic acid (2), the reaction of 1a provides 7-chloro-4-phenylquinoline (3) (78%) together with diphenylquinoline (4) (12%), while 1b reacts in a much more regioselective fashion and provides 3 in 98% isolated yield. Although 1b undergoes a more regioselective Suzuki reaction than 1a, additional important observations are that the overall reaction of 1b with 2 is three times slower than 1a and that the reaction occurs in the absence of tetrabutylammonium bromide. Using optimized reaction conditions, a variety of aryl and vinylboronic acids undergo regioselective Suzuki cross-coupling with 1b to provide the products 7, 10, and 11 in good to excellent yield.Key words: palladium, cross-coupling, regioselectivity, quinolines, boronic acids.


2011 ◽  
Vol 7 ◽  
pp. 310-319 ◽  
Author(s):  
Sanjay R Borhade ◽  
Suresh Babsaheb Waghmode

Palladium supported on nickel ferrite (Pd/NiF2O4) was found to be a highly active catalyst for the Suzuki coupling reaction between various aryl halides and arylboronic acids. The reaction gave excellent yields (70–98%) under ligand free conditions in a 1:1 DMF/H2O solvent mixture, in short reaction times (10–60 min). The catalyst could be recovered easily by applying an external magnetic field. The polyaryls were similarly synthesized.


RSC Advances ◽  
2016 ◽  
Vol 6 (110) ◽  
pp. 108755-108767 ◽  
Author(s):  
Reza Fareghi-Alamdari ◽  
Mohsen Golestanzadeh ◽  
Omid Bagheri

In this study, meso-tetrakis[4-(methoxycarbonyl)phenyl]porphynatopalladium(ii) as a macrocyclic palladium complex was covalently grafted to the surface of graphene oxide (Pd-TMCPP-GO). The prepared catalyst was checked in Suzuki reaction.


RSC Advances ◽  
2014 ◽  
Vol 4 (22) ◽  
pp. 11152-11158 ◽  
Author(s):  
Chaonan Dong ◽  
Lingjuan Zhang ◽  
Xiao Xue ◽  
Huanrong Li ◽  
Zhiyong Yu ◽  
...  

The combination of Pd(TFA)2 and KOH could efficiently catalyze the reaction of β-substituted allylic halides with arylboronic acids in water.


2001 ◽  
Vol 44-45 ◽  
pp. 537-545 ◽  
Author(s):  
H Kosslick ◽  
I Mönnich ◽  
E Paetzold ◽  
H Fuhrmann ◽  
R Fricke ◽  
...  

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