Improved Nickel-Catalyzed Cross-Coupling Reaction Conditions between ortho -Substituted Aryl Iodides/Nonaflates and Alkylzinc Iodides in Solution and in the Solid-Phase

Tetrahedron ◽  
2000 ◽  
Vol 56 (25) ◽  
pp. 4197-4201 ◽  
Author(s):  
Anne Eeg Jensen ◽  
Wolfgang Dohle ◽  
Paul Knochel
2011 ◽  
Vol 2011 (9) ◽  
pp. 1776-1781 ◽  
Author(s):  
Hsin-Lun Kao ◽  
Chin-Keng Chen ◽  
Yu-Jen Wang ◽  
Chin-Fa Lee

Synthesis ◽  
2020 ◽  
Vol 52 (16) ◽  
pp. 2387-2394 ◽  
Author(s):  
Jorge A. Cabezas ◽  
Natasha Ferllini

A regiospecific palladium-catalyzed cross-coupling reaction using the operational equivalent of the dianion 1,3-dilithiopropyne, with aromatic iodides is reported. This reaction gives high yields of 1-propyn-1-yl-benzenes and 2-(propyn-1-yl)thiophenes in the presence of catalytic amounts of palladium(0) or (II) and stoichiometric amounts of copper iodide. No terminal alkyne or allene isomers were detected. Reaction conditions were very mild and several functional groups were tolerated.


Synthesis ◽  
2014 ◽  
Vol 47 (02) ◽  
pp. 181-186 ◽  
Author(s):  
Chin-Fa Lee ◽  
Yi-An Chen ◽  
Satpal Badsara ◽  
Wan-Ting Tsai

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