Arylboronic Acids and Arylpinacolboronate Esters in Suzuki Coupling Reactions Involving Indoles. Partner Role Swapping and Heterocycle Protection

2004 ◽  
Vol 69 (20) ◽  
pp. 6812-6820 ◽  
Author(s):  
Mònica Prieto ◽  
Esther Zurita ◽  
Esmeralda Rosa ◽  
Lourdes Muñoz ◽  
Paul Lloyd-Williams ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids

scholarly journals Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

RSC Advances ◽  
2018 ◽  
Vol 8 (70) ◽  
pp. 40000-40015 ◽  
Author(s):  
Nedra Touj ◽  
Abdullah S. Al-Ayed ◽  
Mathieu Sauthier ◽  
Lamjed Mansour ◽  
Abdel Halim Harrath ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Boronic Acids ◽  
Cytotoxic Activities ◽  
Coupling Reactions ◽  
Component System ◽  
Arylboronic Acids ◽  
Cross Coupling Reaction

The in situ prepared four component system Pd(OAc)2, 1,3-dialkylbenzimidazolium halides 2a–i and 4a–i, K2CO3 under CO atmosphere catalyses carbonylative cross-coupling reaction of 2-bromopyridine with various boronic acids to yield unsymmetrical arylpyridine ketones.

scholarly journals Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

RSC Advances ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 675-675 ◽  
Author(s):  
Nedra Touj ◽  
Abdullah S. Al-Ayed ◽  
Mathieu Sauthier ◽  
Lamjed Mansour ◽  
Abdel Halim Harrath ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Cytotoxic Activities ◽  
Coupling Reactions ◽  
Arylboronic Acids

Correction for ‘Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities’ by Nedra Touj et al., RSC Adv., 2018, 8, 40000–40015.

scholarly journals Arylboronic Acids and Arylpinacolboronate Esters in Suzuki Coupling Reactions Involving Indoles. Partner Role Swapping and Heterocycle Protection.

ChemInform ◽  
2005 ◽  
Vol 36 (6) ◽  
Author(s):  
Monica Prieto ◽  
Esther Zurita ◽  
Esmeralda Rosa ◽  
Lourdes Munoz ◽  
Paul Lloyd-Williams ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids

A well-designed sandwich-like MS/Pd@MS hollow nanosphere for Suzuki coupling reactions of aryl bromides and arylboronic acids

2019 ◽  
Vol 110 ◽  
pp. 107579
Author(s):  
Fangfang Wei ◽  
Jian Liu ◽  
Qiqin Yang ◽  
Yangping Deng ◽  
Shuai Han ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Hollow Nanosphere ◽  
Arylboronic Acids ◽  
Aryl Bromides

scholarly journals Carbonylative Suzuki coupling reactions of aryl iodides with arylboronic acids over Pd/SiC

2015 ◽  
Vol 36 (3) ◽  
pp. 322-327 ◽  
Author(s):  
Yanli Cui ◽  
Xiaoning Guo ◽  
Yingyong Wang ◽  
Xiangyun Guo
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Aryl Iodides

ChemInform Abstract: Pd(OAc)2/2-Aryl-2-oxazolines Catalyzed Suzuki Coupling Reactions of Aryl Bromides and Arylboronic Acids.

ChemInform ◽  
2010 ◽  
Vol 33 (41) ◽  
pp. no-no
Author(s):  
Bin Tao ◽  
David W. Boykin
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Aryl Bromides

scholarly journals Recent progress in application of nanocatalysts for carbonylative Suzuki cross-coupling reactions

RSC Advances ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 2112-2125
Author(s):  
Inci Söğütlü ◽  
Evan Abdulkarim Mahmood ◽  
Saeid Ahmadizadeh Shendy ◽  
Saeideh Ebrahimiasl ◽  
Esmail Vessally
Keyword(s):  
Carbon Monoxide ◽  
Recent Progress ◽  
Cross Coupling ◽  
Suzuki Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Cross Coupling Reactions ◽  
Carbon Carbon Bonds ◽  
Carbon Bonds

Cross-coupling of aryl halides and arylboronic acids in the presence of carbon monoxide, also called carbonylative Suzuki coupling, to form two new carbon–carbon bonds in the production of synthetically and biologically important biaryl ketones, has been widely studied.

Pd(OAc)2/2-aryl-2-oxazolines catalyzed Suzuki coupling reactions of aryl bromides and arylboronic acids

2002 ◽  
Vol 43 (28) ◽  
pp. 4955-4957 ◽  
Author(s):  
Bin Tao ◽  
David W Boykin
Keyword(s):  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acids ◽  
Aryl Bromides
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