Polyaniline-anchored palladium catalyst-mediated Mizoroki-Heck and Suzuki-Miyaura reactions and one-pot Wittig-Heck and Wittig-Suzuki reactions

2014 ◽  
Vol 29 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Heta A. Patel ◽  
Arun L. Patel ◽  
Ashutosh V. Bedekar
Keyword(s):  
Palladium Catalyst ◽  
One Pot ◽  
Suzuki Reactions

Pd-Catalyzed one-pot sequential cross-coupling reactions of tetrabromothiophene

2017 ◽  
Vol 15 (48) ◽  
pp. 10289-10298 ◽  
Author(s):  
Kapil Mohan Saini ◽  
Rakesh K. Saunthwal ◽  
Akhilesh K. Verma
Keyword(s):  
Palladium Catalyst ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Arylboronic Acid ◽  
One Pot ◽  
Cross Coupling Reactions ◽  
Sterically Hindered

Unsymmetrical one-pot sequential cross-coupling reactions of sterically hindered tetrabromothiophene with arylboronic acid and an alkyne/alkene to afford selective bi-, tri-, and tetrasubstituted aryl/alkynyl-thiophenes with the aid of a palladium catalyst were described.

scholarly journals Synthesis of Pentasubstituted 2-Aryl Pyrroles from Boryl and Stannyl Alkynes via One-Pot Sequential Ti-Catalyzed [2+2+1] Pyrrole Synthesis/Cross Coupling Reactions

2020 ◽  
Author(s):  
Yukun Cheng ◽  
Channing Klein ◽  
Ian Tonks
Keyword(s):  
Cross Coupling ◽  
Catalytic Synthesis ◽  
Coupling Reactions ◽  
One Pot ◽  
Suzuki Reactions ◽  
Cross Coupling Reactions ◽  
Substituted Pyrroles

<div> <div> <div> <div> <p>An efficient catalytic synthesis of 2-heteroatom-substituted (9-BBN or SnR3) pyrroles via Ti-catalyzed [2+2+1] heterocoupling of heteroatom-substituted alkynes is reported. The resulting 2-boryl substituted pyrroles can then be used in Suzuki reactions in a 1-pot sequential fashion, resulting in pentasubstituted 2-aryl pyrroles that are inaccessible via previous [2+2+1] heterocoupling strategies. </p> </div> </div> </div> </div>

ChemInform Abstract: Ligand-Free Pd/C-Catalyzed One-Pot, Three-Component Synthesis of Aryl-Substituted Benzimidazoles by Hydrogen-Transfer and Suzuki Reactions in Water.

ChemInform ◽  
2016 ◽  
Vol 47 (14) ◽  
Author(s):  
Chen Xu ◽  
Zhi-Qiang Xiao ◽  
Hong-Mei Li ◽  
Xin Han ◽  
Zhi-Qiang Wang ◽  
...  
Keyword(s):  
Hydrogen Transfer ◽  
One Pot ◽  
Suzuki Reactions ◽  
Ligand Free

scholarly journals Reusable magnetic PdxCoy nanoalloys confined in mesoporous carbons for green Suzuki–Miyaura reactions

RSC Advances ◽  
2018 ◽  
Vol 8 (31) ◽  
pp. 17176-17182 ◽  
Author(s):  
Mohamed Enneiymy ◽  
Claude Le Drian ◽  
Camélia Matei Ghimbeu ◽  
Jean-Michel Becht
Keyword(s):  
Mesoporous Carbons ◽  
One Pot ◽  
Suzuki Reactions

(Pdx–Coy)@MC were prepared in one-pot via an eco-friendly route and used many times for Suzuki reactions in H2O or H2O/EtOH mixture.

Open-Vessel Microwave-Promoted Suzuki Reactions Using Low Levels of Palladium Catalyst:  Optimization and Scale-Up

2006 ◽  
Vol 10 (4) ◽  
pp. 833-837 ◽  
Author(s):  
Nicholas E. Leadbeater ◽  
Victoria A. Williams ◽  
Thomas M. Barnard ◽  
Michael J. Collins
Keyword(s):  
Palladium Catalyst ◽  
Scale Up ◽  
Suzuki Reactions ◽  
Low Levels

One-pot solvothermal synthesis of Pd/Fe3O4 nanocomposite and its magnetically recyclable and efficient catalysis for Suzuki reactions

2012 ◽  
Vol 359 ◽  
pp. 81-87 ◽  
Author(s):  
Shaozhong Li ◽  
Wei Zhang ◽  
Man-Ho So ◽  
Chi-Ming Che ◽  
Runming Wang ◽  
...  
Keyword(s):  
Solvothermal Synthesis ◽  
One Pot ◽  
Suzuki Reactions

Ligand-Free Pd/C-Catalyzed One-Pot, Three-Component Synthesis of Aryl-Substituted Benzimidazoles by Hydrogen-Transfer and Suzuki Reactions in Water

2015 ◽  
Vol 2015 (34) ◽  
pp. 7427-7432 ◽  
Author(s):  
Chen Xu ◽  
Zhi-Qiang Xiao ◽  
Hong-Mei Li ◽  
Xin Han ◽  
Zhi-Qiang Wang ◽  
...  
Keyword(s):  
Hydrogen Transfer ◽  
One Pot ◽  
Suzuki Reactions ◽  
Ligand Free
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