Oxidative Addition of a Strained C–C Bond onto Electron-Rich Rhodium(I) at Room Temperature

2013 ◽  
Vol 135 (19) ◽  
pp. 7142-7145 ◽  
Author(s):  
Yusuke Masuda ◽  
Maki Hasegawa ◽  
Makoto Yamashita ◽  
Kyoko Nozaki ◽  
Naoki Ishida ◽  
...  
2020 ◽  
Vol 49 (17) ◽  
pp. 5416-5419
Author(s):  
S. Azpeitia ◽  
A. J. Martínez-Martínez ◽  
M. A. Garralda ◽  
A. S. Weller ◽  
M. A. Huertos

Rhodium promoted a fast, quantitative and room temperature Si–CH3 bond activation.


2017 ◽  
Vol 46 (36) ◽  
pp. 12015-12018 ◽  
Author(s):  
Lucía García ◽  
Khalidah H. M. Al Furaiji ◽  
David J. D. Wilson ◽  
Jason L. Dutton ◽  
Michael S. Hill ◽  
...  

Reaction of phenylsilane with the ring expanded carbene 6-Mes results in facile Si–H oxidative addition to the carbenic carbon at room temperature and ring opening on heating.


1999 ◽  
Vol 285 (2) ◽  
pp. 277-282 ◽  
Author(s):  
Alejandro J. Arce ◽  
Arquı́medes Karam ◽  
Ysaura De Sanctis ◽  
Mario V. Capparelli ◽  
Antony J. Deeming

2020 ◽  
Vol 39 (3) ◽  
pp. 417-424 ◽  
Author(s):  
Hamid R. Shahsavari ◽  
Reza Babadi Aghakhanpour ◽  
Abbas Biglari ◽  
Maryam Niazi ◽  
Piero Mastrorilli ◽  
...  

2020 ◽  
Vol 117 (35) ◽  
pp. 21058-21064
Author(s):  
Marissa N. Lavagnino ◽  
Tao Liang ◽  
David W. C. MacMillan

The copper-catalyzed arylation of unsaturated nitrogen heterocycles, known as the Ullmann–Goldberg coupling, is a valuable transformation for medicinal chemists, providing a modular disconnection for the rapid diversification of heteroaromatic cores. The utility of the coupling, however, has established limitations arising from a high-barrier copper oxidative addition step, which often necessitates the use of electron-rich ligands, elevated temperatures, and/or activated aryl electrophiles. Herein, we present an alternative aryl halide activation strategy, in which the critical oxidative addition (OA) mechanism has been replaced by a halogen abstraction–radical capture (HARC) sequence that allows the generation of the same Cu(III)-aryl intermediate albeit via a photoredox pathway. This alternative mechanistic paradigm decouples the bond-breaking and bond-forming steps of the catalytic cycle to enable the use of many previously inert aryl bromides. Overall, this mechanism allows access to both traditional C–N adducts at room temperature as well as a large range of previously inaccessible Ullmann–Goldberg coupling products including sterically demandingortho-substituted heteroarenes.


Author(s):  
J. E. Doherty ◽  
A. F. Giamei ◽  
B. H. Kear ◽  
C. W. Steinke

Recently we have been investigating a class of nickel-base superalloys which possess substantial room temperature ductility. This improvement in ductility is directly related to improvements in grain boundary strength due to increased boundary cohesion through control of detrimental impurities and improved boundary shear strength by controlled grain boundary micros true tures.For these investigations an experimental nickel-base superalloy was doped with different levels of sulphur impurity. The micros tructure after a heat treatment of 1360°C for 2 hr, 1200°C for 16 hr consists of coherent precipitates of γ’ Ni3(Al,X) in a nickel solid solution matrix.


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