aryl chloride silylation

Author(s):  
R.B. Lincoln
Keyword(s):  
2020 ◽  
Vol 646 (15) ◽  
pp. 1336-1341 ◽  
Author(s):  
Xue-Fang Gong ◽  
Ling-Yan Zhang ◽  
Hui-Xin Zhang ◽  
Yu-Meng Cui ◽  
Fen-Chun Jin ◽  
...  

2020 ◽  
Vol 59 (34) ◽  
pp. 15179-15187
Author(s):  
Hikaru Matsumoto ◽  
Yu Hoshino ◽  
Tomohiro Iwai ◽  
Masaya Sawamura ◽  
Yoshiko Miura

2014 ◽  
Vol 67 (3) ◽  
pp. 374 ◽  
Author(s):  
Jean E. Glover ◽  
Paul G. Plieger ◽  
Gareth J. Rowlands

An enantiomerically pure planar chiral pyridine-based palladacycle was prepared from [2.2]paracyclophane in just four steps. The palladacycle shows potential in catalysis, mediating the Suzuki coupling of an aryl chloride. It also permits the ortho bromination of [2.2]paracyclophane, a reaction that can be hard to achieve selectively.


2001 ◽  
Vol 123 (51) ◽  
pp. 12905-12906 ◽  
Author(s):  
Luis M. Alcazar-Roman ◽  
John F. Hartwig

2004 ◽  
Vol 45 (39) ◽  
pp. 7315-7317 ◽  
Author(s):  
Demet Astley ◽  
Hava Saygı ◽  
Sibel Gezer ◽  
Stephen T. Astley

2013 ◽  
Vol 49 (91) ◽  
pp. 10715 ◽  
Author(s):  
Fareed Bhasha Sayyed ◽  
Yasushi Tsuji ◽  
Shigeyoshi Sakaki

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