Triallyl(aryl)silanes serve as a convenient agent for silicon-based cross-coupling reaction of aryl halides

2003 ◽  
Vol 687 (2) ◽  
pp. 570-573 ◽  
Author(s):  
Yoshiaki Nakao ◽  
Takuro Oda ◽  
Akhila K. Sahoo ◽  
Tamejiro Hiyama
Synlett ◽  
2017 ◽  
Vol 28 (15) ◽  
pp. 1873-1884 ◽  
Author(s):  
Yasunori Minami ◽  
Tamejiro Hiyama ◽  
Takeshi Komiyama

The silicon-based cross-coupling reaction has attracted much attention over recent decades because there are many advantages in using organosilicon compounds. However, the use of reagents with a triorganosilyl group as a key function remains to be established. This account summarizes our recent progress in cross-coupling chemistry with such silyl reagents.1 Introduction2 Preparation of HOMSi Reagents from Aryl Bromides and Disilanes3 HOMSi Reagents from Heteroaromatics and Hydrosilanes4 Cross-Coupling Polymerization with HOMSi Reagents5 Cross-Coupling with Aryl(triethyl)silanes6 Amination of Aryl Halides with N-TMS-Amines7 Conclusion and Perspective


ChemInform ◽  
2004 ◽  
Vol 35 (16) ◽  
Author(s):  
Yoshiaki Nakao ◽  
Takuro Oda ◽  
Akhila K. Sahoo ◽  
Tamejiro Hiyama

ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Anns Maria Thomas ◽  
Sujatha Asha ◽  
K. S.. Sindhu ◽  
Gopinathan Anilkumar

2020 ◽  
Vol 56 (74) ◽  
pp. 10942-10945
Author(s):  
Yichao Gu ◽  
Xueliang Sun ◽  
Bin Wan ◽  
Zhuoer Lu ◽  
Yanghui Zhang

A palladium-catalyzed cross-coupling reaction of aryl halides with 2-chlorobenzoic acids has been developed through C(sp3)–H activation, which provides an innovative method for the synthesis of 9,10-dihydrophenanthren.


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