Ligand‐free Palladium‐Catalyzed Carbonylative Suzuki Coupling of Aryl Iodides in Aqueous CH 3 CN with Sub‐stoichiometric Amount of Mo(CO) 6 as CO Source

2019 ◽  
Vol 361 (9) ◽  
pp. 2117-2123 ◽  
Author(s):  
Nan Sun ◽  
Qingxia Sun ◽  
Wei Zhao ◽  
Liqun Jin ◽  
Baoxiang Hu ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Stoichiometric Amount ◽  
Aryl Iodides ◽  
Ligand Free ◽  
Palladium Catalyzed

Ligand-free palladium catalyzed phosphorylation of aryl iodides

2016 ◽  
Vol 57 (3) ◽  
pp. 348-350 ◽  
Author(s):  
Najmeh Nowrouzi ◽  
Saba Keshtgar ◽  
Enayatollah Bahman Jahromi
Keyword(s):  
Aryl Iodides ◽  
Ligand Free ◽  
Palladium Catalyzed

scholarly journals Synthesis of aryl substituted indanones and indenes via a highly efficient ligand-free palladium-catalyzed Suzuki coupling process

ARKIVOC ◽  
2016 ◽  
Vol 2016 (4) ◽  
pp. 306-327 ◽  
Author(s):  
Yuming Song ◽  
Yamei Xie ◽  
Minjian Chen ◽  
Jingping Qu ◽  
Hongfan Hu ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Coupling Process ◽  
Highly Efficient ◽  
Ligand Free ◽  
Palladium Catalyzed

ChemInform Abstract: Ligand-Free Palladium Catalyzed Phosphorylation of Aryl Iodides.

ChemInform ◽  
2016 ◽  
Vol 47 (19) ◽  
Author(s):  
Najmeh Nowrouzi ◽  
Saba Keshtgar ◽  
Enayatollah Bahman Jahromi
Keyword(s):  
Aryl Iodides ◽  
Ligand Free ◽  
Palladium Catalyzed

Synthesis of S-aryl thioesters via palladium-catalyzed thiocarbonylation of aryl iodides and aryl sulfonyl hydrazides

2020 ◽  
Vol 7 (19) ◽  
pp. 2938-2943
Author(s):  
Yeojin Kim ◽  
Kwang Ho Song ◽  
Sunwoo Lee
Keyword(s):  
Aryl Iodide ◽  
Aryl Iodides ◽  
Palladium Catalyzed

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

Palladium-catalyzed carbonylative transformation of aryl iodides and sulfonyl chlorides: convenient access to thioesters

2020 ◽  
Vol 7 (6) ◽  
pp. 885-889 ◽  
Author(s):  
Xinxin Qi ◽  
Zhi-Peng Bao ◽  
Xiao-Feng Wu
Keyword(s):  
Sulfonyl Chlorides ◽  
Aryl Iodides ◽  
Palladium Catalyzed ◽  
Convenient Access

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

Palladium-Catalyzed Asymmetric Annulation Between Aryl Iodides and Racemic Epoxides Using a Chiral Norbornene Cocatalyst

2018 ◽  
Author(s):  
Guangbin Dong ◽  
Renhe Li
Keyword(s):  
Isopropyl Ester ◽  
Synthetic Route ◽  
Initial Development ◽  
Aryl Iodides ◽  
Palladium Catalyzed

Herein, we describe our initial development of an asymmetric Pd-catalyzed annulation between aryl iodides and racemic epoxides for synthesis of 2,3-dihydrobenzofurans using a chiral norbornene cocatalyst. A series of enantiopure ester-, amide- and imide-substituted norbornenes have been prepared with a reliable synthetic route. Promising enantioselectivity (42-45% ee) has been observed using the isopropyl ester-substituted norbornene (N1*) and the amide-substituted norbornene (N7*).

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