scholarly journals SYNTHESIS OF AROMATIC THIOLS FROM ARYL IODIDES AND THIOUREA BY MEANS OF NICKEL CATALYST

1985 ◽  
Vol 14 (9) ◽  
pp. 1307-1308 ◽  
Author(s):  
Kentaro Takagi
Keyword(s):  
Nickel Catalyst ◽  
Aryl Iodides ◽  
Aromatic Thiols

scholarly journals SYNTHESIS OF ARYL IODIDES FROM ARYL HALIDES AND POTASSIUM IODIDE BY MEANS OF NICKEL CATALYST

1978 ◽  
Vol 7 (2) ◽  
pp. 191-192 ◽  
Author(s):  
Kentaro Takagi ◽  
Naomi Hayama ◽  
Tadashi Okamoto
Keyword(s):  
Nickel Catalyst ◽  
Potassium Iodide ◽  
Aryl Halides ◽  
Aryl Iodides

scholarly journals SYNTHESIS OF BIARYLS FROM ARYL IODIDES AND ZINC POWDER BY MEANS OF NICKEL CATALYST

1979 ◽  
Vol 8 (8) ◽  
pp. 917-918 ◽  
Author(s):  
Kentaro Takagi ◽  
Naomi Hayama ◽  
Saburo Inokawa
Keyword(s):  
Nickel Catalyst ◽  
Zinc Powder ◽  
Aryl Iodides

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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