Unprecedented coordination of a silicon-chlorine bond to a transition metal: synthesis and structure of [rac-C2H4(indenyl)2Zr{CH(SiMe2Cl)(SiMe3)}][Al2Cl6.5Me0.5] formed by reversible silicon-carbon bond activation

1992 ◽  
Vol 11 (3) ◽  
pp. 1193-1201 ◽  
Author(s):  
Andrew D. Horton ◽  
A. Guy Orpen
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.


Author(s):  
Long Yang ◽  
Wuxin Zhou ◽  
Qiang Li ◽  
Xiangge Zhou

Carbon−carbon bond activation is one of the most challenging and important research areas in organic chemistry. Selective C−C bond activation of unstrained substrates is difficult to achieve owing to its...


2012 ◽  
Vol 31 (9) ◽  
pp. 3539-3550 ◽  
Author(s):  
Muhieddine Safa ◽  
Michael C. Jennings ◽  
Richard J. Puddephatt

2010 ◽  
Vol 46 (16) ◽  
pp. 2811 ◽  
Author(s):  
Muhieddine Safa ◽  
Michael C. Jennings ◽  
Richard J. Puddephatt

Sign in / Sign up

Export Citation Format

Share Document