Catalytic allylic functionalization via π-allyl palladium chemistry

2019 ◽  
Vol 17 (38) ◽  
pp. 8647-8672 ◽  
Author(s):  
Rodney A. Fernandes ◽  
Jothi L. Nallasivam

This review highlights the palladium-catalyzed allylic C–H functionalizations via π-allyl palladium reported from early 2014 to present date.

2004 ◽  
Vol 08 (01) ◽  
pp. 93-102 ◽  
Author(s):  
Jun-ichiro Setsune

Palladium-catalyzed reactions such as Sonogashira coupling, Suzuki coupling, Stille coupling, Heck reactions, and Glaser-Hey oxidation were used to construct porphyrin modules of nano-scale molecular size in recent years. Recent developments in the supramolecular assembly of porphyrins and Pd (II) and in the organopalladium complexes of various porphyrins are also summarized.


1988 ◽  
Vol 29 (45) ◽  
pp. 5739-5742 ◽  
Author(s):  
Vittorio Farina ◽  
Stephen R. Baker ◽  
Daniel A. Benigni ◽  
Chester Sapino

2020 ◽  
Vol 7 (19) ◽  
pp. 2938-2943
Author(s):  
Yeojin Kim ◽  
Kwang Ho Song ◽  
Sunwoo Lee

Aryl sulfonyl hydrazide reacted with aryl iodide in the presence of CO to give the corresponding S-aryl thioesters.


2020 ◽  
Vol 7 (6) ◽  
pp. 885-889 ◽  
Author(s):  
Xinxin Qi ◽  
Zhi-Peng Bao ◽  
Xiao-Feng Wu

A palladium-catalyzed carbonylative transformation of aryl iodides and sulfonyl chlorides to thioesters has been studied.


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