A palladium-catalyzed reaction of a .pi.-allyl ligand with a nucleophile. An MO study about a feature of the reaction and a ligand effect on the reactivity

1980 ◽  
Vol 102 (12) ◽  
pp. 4062-4069 ◽  
Author(s):  
Shigeyoshi Sakaki ◽  
Masahiro Nishikawa ◽  
Akira Ohyoshi
2014 ◽  
Vol 53 (27) ◽  
pp. 7068-7073 ◽  
Author(s):  
Antonio Misale ◽  
Supaporn Niyomchon ◽  
Marco Luparia ◽  
Nuno Maulide

2010 ◽  
Vol 16 (20) ◽  
pp. 5863-5867 ◽  
Author(s):  
Stéphanie Jaegli ◽  
William Erb ◽  
Pascal Retailleau ◽  
Jean-Pierre Vors ◽  
Luc Neuville ◽  
...  

2014 ◽  
Vol 34 (1) ◽  
pp. 198-205 ◽  
Author(s):  
Masayuki Wakioka ◽  
Yuki Nakamura ◽  
Michelle Montgomery ◽  
Fumiyuki Ozawa

ChemInform ◽  
2014 ◽  
Vol 45 (51) ◽  
pp. no-no
Author(s):  
Antonio Misale ◽  
Supaporn Niyomchon ◽  
Marco Luparia ◽  
Nuno Maulide

ChemInform ◽  
2010 ◽  
Vol 41 (40) ◽  
pp. no-no
Author(s):  
Stephanie Jaegli ◽  
William Erb ◽  
Pascal Retailleau ◽  
Jean-Pierre Vors ◽  
Luc Neuville ◽  
...  

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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