One-pot Synthesis of Substituted Quinolines by Iridium-catalyzed Three-component Coupling Reaction

2005 ◽  
Vol 34 (1) ◽  
pp. 106-107 ◽  
Author(s):  
Takeyuki Igarashi ◽  
Takashi Inada ◽  
Tadao Sekioka ◽  
Takayuki Nakajima ◽  
Isao Shimizu
ChemInform ◽  
2005 ◽  
Vol 36 (24) ◽  
Author(s):  
Takeyuki Igarashi ◽  
Takashi Inada ◽  
Tadao Sekioka ◽  
Takayuki Nakajima ◽  
Isao Shimizu

CrystEngComm ◽  
2020 ◽  
Vol 22 (15) ◽  
pp. 2642-2648 ◽  
Author(s):  
Ming-Yu Dou ◽  
Xian-Qiang Huang ◽  
Guo-Yu Yang

Two silver-polyoxometalates [Ag3L2(DMSO)2][PW12O40]·4DMSO (1) and [(Ag2L2)2][SiW12O40]·10DMSO·2H2O (2) are made and 1 shows good catalytic activities for three-component coupling reaction.


2021 ◽  
Vol 6 (17) ◽  
pp. 4404-4410
Author(s):  
Partha Sarathi Bera ◽  
Shyam Sundar Mondal ◽  
Rima Das ◽  
Subhas Ghosal ◽  
Tanmoy Kumar Saha

Synthesis ◽  
2019 ◽  
Vol 51 (11) ◽  
pp. 2323-2330
Author(s):  
Norio Sakai ◽  
Hiromu Maeda ◽  
Yohei Ogiwara

A copper-catalyzed three-component coupling reaction of aryl iodides, hexamethyldisilathiane and alkyl benzoates leading to alkyl aryl sulfides has been demonstrated. A disilathiane acted as both a sulfur source and a promoter of the sulfidation, and the alkyl moiety of the alkyl benzoate was effectively introduced on one side of the sulfide. Moreover, we found that the protocol can be expanded to the preparation of ethyl phenyl selenide with diphenyl diselenide.


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