Metal catalysis in organic reactions. 18. Stereochemistry of the transition-metal catalyzed cross-coupling of (S)-1-bromo-3-methyl-1,2-pentadiene with isobutylmetal compounds.

1986 ◽  
Vol 29 (9) ◽  
pp. 1067-1068
Author(s):  
A Caporusso
2020 ◽  
Vol 24 (3) ◽  
pp. 231-264 ◽  
Author(s):  
Kevin H. Shaughnessy

Phosphines are widely used ligands in transition metal-catalyzed reactions. Arylphosphines, such as triphenylphosphine, were among the first phosphines to show broad utility in catalysis. Beginning in the late 1990s, sterically demanding and electronrich trialkylphosphines began to receive attention as supporting ligands. These ligands were found to be particularly effective at promoting oxidative addition in cross-coupling of aryl halides. With electron-rich, sterically demanding ligands, such as tri-tertbutylphosphine, coupling of aryl bromides could be achieved at room temperature. More importantly, the less reactive, but more broadly available, aryl chlorides became accessible substrates. Tri-tert-butylphosphine has become a privileged ligand that has found application in a wide range of late transition-metal catalyzed coupling reactions. This success has led to the use of numerous monodentate trialkylphosphines in cross-coupling reactions. This review will discuss the general properties and features of monodentate trialkylphosphines and their application in cross-coupling reactions of C–X and C–H bonds.


2021 ◽  
Author(s):  
Cong Ma ◽  
Ping Fang ◽  
Dong Liu ◽  
Ke-Jin Jiao ◽  
Pei-Sen Gao ◽  
...  

Abstract: Transition metal-catalyzed organic electrochemistry is a rapidly growing research area owing in part of the ability of metal catalysts to alter the selectivity of a given transformation. This conversion...


2006 ◽  
Vol 71 (7) ◽  
pp. 2802-2810 ◽  
Author(s):  
Susana López ◽  
Francisco Fernández-Trillo ◽  
Pilar Midón ◽  
Luis Castedo ◽  
Carlos Saá

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