Effects of Ionic Liquids on Pd-Catalysed Carbon–Carbon Bond Formation

2006 ◽  
Vol 2006 (17) ◽  
pp. 3791-3802 ◽  
Author(s):  
Vincenzo Calò ◽  
Angelo Nacci ◽  
Antonio Monopoli
ChemInform ◽  
2005 ◽  
Vol 36 (1) ◽  
Author(s):  
Vincenzo Calo ◽  
Angelo Nacci ◽  
Antonio Monopoli

2001 ◽  
Vol 56 (9-10) ◽  
pp. 702-706 ◽  
Author(s):  
Vincenzo Calò ◽  
Angelo Nacci

Abstract Rates of Heck-type reactions, catalysed by a Pd-catalyst with benzothiazole carbene as ligands, are strongly influenced by tetrabutylammonium bromide utilized as solvent.


ChemInform ◽  
2014 ◽  
Vol 45 (3) ◽  
pp. no-no
Author(s):  
Francisco Ramon Fortea-Perez ◽  
Isabel Schlegel ◽  
Miguel Julve ◽  
Donatella Armentano ◽  
Giovanni De Munno ◽  
...  

ChemInform ◽  
2006 ◽  
Vol 37 (48) ◽  
Author(s):  
Vincenzo Calo ◽  
Angelo Nacci ◽  
Antonio Monopoli

2007 ◽  
Vol 2007 (30) ◽  
pp. 5095-5100 ◽  
Author(s):  
Chengfeng Ye ◽  
Ji-Chang Xiao ◽  
Brendan Twamley ◽  
Aaron D. LaLonde ◽  
M. Grant Norton ◽  
...  

2013 ◽  
Vol 743 ◽  
pp. 102-108 ◽  
Author(s):  
Francisco Ramón Fortea-Pérez ◽  
Isabel Schlegel ◽  
Miguel Julve ◽  
Donatella Armentano ◽  
Giovanni De Munno ◽  
...  

2018 ◽  
Author(s):  
Mohit Kapoor ◽  
Pratibha Chand-Thakuri ◽  
Michael Young

Carbon-carbon bond formation by transition metal-catalyzed C–H activation has become an important strategy to fabricate new bonds in a rapid fashion. Despite the pharmacological importance of <i>ortho</i>-arylbenzylamines, however, effective <i>ortho</i>-C–C bond formation from C–H bond activation of free primary and secondary benzylamines using Pd<sup>II</sup> remains an outstanding challenge. Presented herein is a new strategy for constructing <i>ortho</i>-arylated primary and secondary benzylamines mediated by carbon dioxide (CO<sub>2</sub>). The use of CO<sub>2</sub> is critical to allowing this transformation to proceed under milder conditions than previously reported, and that are necessary to furnish free amine products that can be directly used or elaborated without the need for deprotection. In cases where diarylation is possible, a chelate effect is demonstrated to facilitate selective monoarylation.


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