Unexpected Intramolecular Oxidative Addition:  Novel Synthetic Route to High-Valent Group 4 Metallacarboranes Bearing aη6- orη7-Carboranyl Ligand

2002 ◽  
Vol 21 (16) ◽  
pp. 3311-3313 ◽  
Author(s):  
Yaorong Wang ◽  
Haiping Wang ◽  
Hung-Wing Li ◽  
Zuowei Xie



2013 ◽  
Vol 42 (39) ◽  
pp. 14168 ◽  
Author(s):  
Tiziana Funaioli ◽  
Fabio Marchetti ◽  
Guido Pampaloni ◽  
Stefano Zacchini




2006 ◽  
pp. 4359-4370 ◽  
Author(s):  
Antonio Otero ◽  
Juan Fernández-Baeza ◽  
Antonio Antiñolo ◽  
Juan Tejeda ◽  
Agustín Lara-Sánchez ◽  
...  


Science ◽  
2018 ◽  
Vol 360 (6392) ◽  
pp. 1010-1014 ◽  
Author(s):  
Chip Le ◽  
Tiffany Q. Chen ◽  
Tao Liang ◽  
Patricia Zhang ◽  
David W. C. MacMillan

Transition metal–catalyzed arene functionalization has been widely used for molecular synthesis over the past century. In this arena, copper catalysis has long been considered a privileged platform due to the propensity of high-valent copper to undergo reductive elimination with a wide variety of coupling fragments. However, the sluggish nature of oxidative addition has limited copper’s capacity to broadly facilitate haloarene coupling protocols. Here, we demonstrate that this copper oxidative addition problem can be overcome with an aryl radical–capture mechanism, wherein the aryl radical is generated through a silyl radical halogen abstraction. This strategy was applied to a general trifluoromethylation of aryl bromides through dual copper-photoredox catalysis. Mechanistic studies support the formation of an open-shell aryl species.



2014 ◽  
Vol 33 (11) ◽  
pp. 2914-2918 ◽  
Author(s):  
Eric J. Derrah ◽  
Stefan Warsink ◽  
Jeroen J. M. de Pater ◽  
Yves Cabon ◽  
Irena Reboule ◽  
...  




2013 ◽  
Vol 52 (12) ◽  
pp. 6944-6950 ◽  
Author(s):  
Erandi Bernabé-Pablo ◽  
Vojtech Jancik ◽  
Mónica Moya-Cabrera


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