An Efficient Catalyst System for Palladium(0)-Catalyzed Cross-Coupling of Aryltrialkoxysilanes with Aryl Halides.

ChemInform ◽  
2006 ◽  
Vol 37 (18) ◽  
Author(s):  
Miki Murata ◽  
Syo Yoshida ◽  
Shin-ichiro Nirei ◽  
Shinji Watanabe ◽  
Yuzuru Masuda
Keyword(s):  
Cross Coupling ◽  
Catalyst System ◽  
Aryl Halides ◽  
Efficient Catalyst

The Suzuki–Miyaura reaction of BPin-substituted F-BODIPYs with aryl halides

2021 ◽  
pp. 1-8
Author(s):  
Craig D. Smith ◽  
Alison Thompson
Keyword(s):  
Functional Groups ◽  
Cross Coupling ◽  
Catalyst System ◽  
Aryl Halides ◽  
Efficient Catalyst

F-BODIPYs substituted with BPin functionality have been coupled to aryl halides using a mild and efficient catalyst system involving Pd2(dba)3 and XPhos. The methodology enables the Suzuki–Miyaura cross-coupling of electron-rich, electron-poor, and sterically encumbered BPin-substituted F-BODIPYs to aryl halides bearing various functional groups, thus presenting an opportunity for the preparation of highly functionalised F-BODIPYs without need for the corresponding aryl moiety to be available in borylated form.

Pd/Indanone-Based Ligands: An Efficient Catalyst System for Ullmann­-Type, Suzuki–Miyaura, and Mizoroki–Heck Cross-Coupling Reactions with Aryl Tosylates and Aryl Halides

Synthesis ◽  
2017 ◽  
Vol 49 (18) ◽  
pp. 4372-4382 ◽  
Author(s):  
Mohammed Waheed ◽  
Naseem Ahmed
Keyword(s):  
Catalytic Activity ◽  
Cross Coupling ◽  
Catalyst System ◽  
Aryl Halides ◽  
Maximum Efficiency ◽  
High Catalytic Activity ◽  
Coupling Reactions ◽  
Efficient Catalyst ◽  
Cross Coupling Reactions ◽  
Aryl Tosylates

2-Hydroxyindan-1-ones have been efficiently synthesized and successfully applied as ligands in Pd-catalyzed Ullmann type, Suzuki–Miyaura, and Mizoroki–Heck cross-coupling reactions with aryl tosylates and aryl halides. The ligands are air- and moisture-stable and have shown high catalytic activity with Pd(OAc)2 in these cross-coupling reactions. The system tolerates a variety of functional groups in the product and can be re-used at least three times with maximum efficiency.

An Efficient Catalyst System for Palladium(0)-Catalyzed Cross-Coupling of Aryltrialkoxysilanes with Aryl Halides

Synlett ◽  
2006 ◽  
pp. 0118-0120 ◽  
Author(s):  
Miki Murata ◽  
Syo Yoshida ◽  
Shin-ichiro Nirei ◽  
Shinji Watanabe ◽  
Yuzuru Masuda
Keyword(s):  
Cross Coupling ◽  
Catalyst System ◽  
Aryl Halides ◽  
Efficient Catalyst

Magnetic CuFe2O4 Nanoparticles as an Efficient Catalyst for CO Cross-Coupling of Phenols with Aryl Halides

ChemCatChem ◽  
2010 ◽  
Vol 3 (1) ◽  
pp. 146-149 ◽  
Author(s):  
Rongzhao Zhang ◽  
Jianming Liu ◽  
Shoufeng Wang ◽  
Jianzhong Niu ◽  
Chungu Xia ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Aryl Halides ◽  
Efficient Catalyst

ChemInform Abstract: CuS/Fe: A Novel and Highly Efficient Catalyst System for Coupling Reaction of Aryl Halides with Diaryl Diselenides.

ChemInform ◽  
2011 ◽  
Vol 42 (8) ◽  
pp. no-no
Author(s):  
Yaming Li ◽  
Huifeng Wang ◽  
Xiaoying Li ◽  
Tao Chen ◽  
Defeng Zhao
Keyword(s):  
Coupling Reaction ◽  
Catalyst System ◽  
Aryl Halides ◽  
Efficient Catalyst ◽  
Highly Efficient

CuS/Fe: a novel and highly efficient catalyst system for coupling reaction of aryl halides with diaryl diselenides

Tetrahedron ◽  
2010 ◽  
Vol 66 (45) ◽  
pp. 8583-8586 ◽  
Author(s):  
Yaming Li ◽  
Huifeng Wang ◽  
Xiaoying Li ◽  
Tao Chen ◽  
Defeng Zhao
Keyword(s):  
Coupling Reaction ◽  
Catalyst System ◽  
Aryl Halides ◽  
Efficient Catalyst ◽  
Highly Efficient

CuI/1,10-phenanthroline: An efficient Catalyst System for the Cyanation of Aryl Halides

2007 ◽  
Vol 2007 (8) ◽  
pp. 484-485 ◽  
Author(s):  
Yi-Zhong Zhu ◽  
Chun Cai
Keyword(s):  
Functional Groups ◽  
Catalyst System ◽  
Aryl Halides ◽  
Potassium Hexacyanoferrate ◽  
Efficient Catalyst ◽  
Aryl Nitriles ◽  
Wide Range

Aryl nitriles have been prepared in good yields from the corresponding aryl halides with potassium hexacyanoferrate(II) using CuI/1,10-phenanthroline as the catalyst system. Furthermore, the reaction is compatible with a wide range of functional groups including nitro and carbonyl substituents.

An efficient indenyl-derived phosphine ligand for the Suzuki–Miyaura coupling of sterically hindered aryl halides

2016 ◽  
Vol 14 (20) ◽  
pp. 4664-4668 ◽  
Author(s):  
Yan Liu ◽  
Hui Peng ◽  
Jia Yuan ◽  
Meng-Qi Yan ◽  
Xue Luo ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Boronic Acids ◽  
Phosphine Ligand ◽  
Aryl Halides ◽  
Efficient Catalyst ◽  
Highly Efficient ◽  
Cross Coupling Reaction ◽  
Sterically Hindered

An air-stable aryl substituted indenyl phosphine used in combination with Pd(OAc)2 provides a highly efficient catalyst for the Suzuki–Miyaura cross-coupling reaction of sterically hindered aryl halides with aryl boronic acids.

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