Palladium-mediated Suzuki-Miyaura Cross-Coupling Reaction of Potassium Boc-protected aminomethyltrifluoroborate with DNA-Conjugated aryl bromides for DNA-Encoded chemical library synthesis

2020 ◽  
Vol 533 (2) ◽  
pp. 209-214 ◽  
Author(s):  
Yi Qu ◽  
Sixiu Liu ◽  
Huanan Wen ◽  
Yanfen Xu ◽  
Yulong An ◽  
...  
ChemInform ◽  
2004 ◽  
Vol 35 (39) ◽  
Author(s):  
Shunji Ito ◽  
Tomomi Terazono ◽  
Takahiro Kubo ◽  
Tetsuo Okujima ◽  
Noboru Morita ◽  
...  

Synthesis ◽  
2001 ◽  
Vol 2001 (15) ◽  
pp. 2231-2233 ◽  
Author(s):  
Miki Murata ◽  
Ryuta Shimazaki ◽  
Shinji Watanabe ◽  
Yuzuru Masuda

2019 ◽  
Vol 21 (2) ◽  
pp. 69-74 ◽  
Author(s):  
Eduardo de Pedro Beato ◽  
Julián Priego ◽  
Adrián Gironda-Martínez ◽  
Fernando González ◽  
Jesús Benavides ◽  
...  

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


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