Sonogashira (Cu and amine free) and Suzuki coupling in air catalyzed via nanoparticles formed in situ from Pd(ii) complexes of chalcogenated Schiff bases of 1-naphthaldehyde and their reduced forms

2017 ◽  
Vol 46 (44) ◽  
pp. 15235-15248 ◽  
Author(s):  
Renu Bhaskar ◽  
Alpesh K. Sharma ◽  
Manoj K. Yadav ◽  
Ajai K. Singh
Keyword(s):  
Schiff Bases ◽  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Mild Conditions ◽  
Reduced Forms

The activation of the coupling reactions with the Pd(ii)-complexes (0.05–0.01 mol% loading) is significant in 1–2 h under mild conditions.

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.

Palladium(ii)-(E,N,E) pincer ligand (E = S/Se/Te) complex catalyzed Suzuki coupling reactions in water via in situ generated palladium quantum dots

2013 ◽  
Vol 42 (48) ◽  
pp. 16939 ◽  
Author(s):  
Satyendra Kumar ◽  
Gyandshwar K. Rao ◽  
Arun Kumar ◽  
Mahabir P. Singh ◽  
Ajai Kumar Singh
Keyword(s):  
Quantum Dots ◽  
Suzuki Coupling ◽  
Coupling Reactions ◽  
Pincer Ligand

scholarly journals Denitrogenative Suzuki and carbonylative Suzuki coupling reactions of benzotriazoles with boronic acids

2017 ◽  
Vol 8 (5) ◽  
pp. 3852-3857 ◽  
Author(s):  
Yuanhao Wang ◽  
Yunfei Wu ◽  
Yuanhe Li ◽  
Yefeng Tang
Keyword(s):  
Suzuki Coupling ◽  
Boronic Acids ◽  
Coupling Reactions ◽  
Suzuki Reactions ◽  
Palladium Catalyzed

Palladium-catalyzed denitrogenative Suzuki and carbonylative Suzuki reactions of benzotriazoles with boronic acids have been achieved through the in situ generation of ortho-amino-arenediazonium species.

scholarly journals Chalcogenated Schiff bases: Complexation with palladium(II) and Suzuki coupling reactions

2012 ◽  
Vol 124 (6) ◽  
pp. 1245-1253 ◽  
Author(s):  
PRADHUMN SINGH ◽  
G K RAO ◽  
MOHD SALMAN KARIM ◽  
AJAI K SINGH
Keyword(s):  
Schiff Bases ◽  
Suzuki Coupling ◽  
Coupling Reactions

ChemInform Abstract: Chalcogenated Schiff Bases: Complexation with Palladium(II) and Suzuki Coupling Reactions.

ChemInform ◽  
2013 ◽  
Vol 44 (18) ◽  
pp. no-no
Author(s):  
Pradhumn Singh ◽  
G. K. Rao ◽  
Mohd Salman Karim ◽  
Ajai K. Singh
Keyword(s):  
Schiff Bases ◽  
Suzuki Coupling ◽  
Coupling Reactions
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