Straightforward access to aryl-substituted/fused 1,3-dithiole-2-chalcogenones by Cu-catalyzed C–S coupling between aryl iodides and zinc–thiolate complex (TBA)2[Zn(DMIT)2]

RSC Advances ◽  
2013 ◽  
Vol 3 (26) ◽  
pp. 10193 ◽  
Author(s):  
Jibin Sun ◽  
Xiaofeng Lu ◽  
Jiafeng Shao ◽  
Zili Cui ◽  
Yu Shao ◽  
...  
Keyword(s):  
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.


2018 ◽  
Author(s):  
Guangbin Dong ◽  
Renhe Li

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*).


2021 ◽  
Vol 40 (4) ◽  
pp. 482-489
Author(s):  
Yafei Li ◽  
Yan Dang ◽  
Dawei Li ◽  
Huifen Pan ◽  
Liang Zhang ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Travis DeLano ◽  
Sara Dibrell ◽  
Caitlin R. Lacker ◽  
Adam Pancoast ◽  
Kelsey Poremba ◽  
...  

An asymmetric reductive cross-coupling of α-chloroesters and (hetero)aryl iodides is reported. This nickel-catalyzed reaction proceeds with a chiral BiOX ligand under mild conditions, affording α-arylesters in good yields and enantioselectivities....


ChemInform ◽  
2009 ◽  
Vol 40 (40) ◽  
Author(s):  
Zhiyong Wang ◽  
Qiuping Ding ◽  
Xiaodan He ◽  
Jie Wu
Keyword(s):  

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