ChemInform Abstract: Suzuki Cross-Coupling of Aryl Halides with Phenylboronic Acid Catalyzed by an Amidoxime Fibres-Nickel(0) Complex.

ChemInform ◽  
2014 ◽  
Vol 45 (6) ◽  
pp. no-no
Author(s):  
Zhi-Chuan Wu ◽  
Ye-Neng Lu ◽  
Yi-Ming Ren ◽  
Zhi-Ming Chen ◽  
Ting-Xian Tao
Keyword(s):  
Phenylboronic Acid ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Acid Catalyzed

Suzuki Cross-Coupling of Aryl Halides with Phenylboronic Acid Catalysed by an Amidoxime Fibres-Nickel(0) Complex

2013 ◽  
Vol 37 (8) ◽  
pp. 451-454 ◽  
Author(s):  
Zhi-Chuan Wu ◽  
Ye-Neng Lu ◽  
Yi-Ming Ren ◽  
Zhi-Ming Chen ◽  
Ting-Xian Tao
Keyword(s):  
Phenylboronic Acid ◽  
Cross Coupling ◽  
Aryl Halides

Magnetic Fe-Ni Alloy Catalyzed Suzuki Cross-Coupling Reactions of Aryl Halides with Phenylboronic Acid

ChemCatChem ◽  
2012 ◽  
Vol 5 (1) ◽  
pp. 142-145 ◽  
Author(s):  
Rongzhao Zhang ◽  
Chengxia Miao ◽  
Shoufeng Wang ◽  
Chungu Xia ◽  
Wei Sun
Keyword(s):  
Phenylboronic Acid ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Ni Alloy

Proline-functionalized chitosan–palladium(ii) complex, a novel nanocatalyst for C–C bond formation in water

RSC Advances ◽  
2015 ◽  
Vol 5 (31) ◽  
pp. 24742-24748 ◽  
Author(s):  
A. R. Hajipour ◽  
E. Boostani ◽  
F. Mohammadsaleh
Keyword(s):  
Phenylboronic Acid ◽  
Bond Formation ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Environmentally Friendly ◽  
Aryl Halides ◽  
Heterogeneous Nanocatalyst ◽  
Cross Coupling Reaction

An environmentally friendly palladium-based catalyst supported on proline-functionalized chitosan was successfully prepared and evaluated as a heterogeneous nanocatalyst in the Suzuki cross-coupling reaction of various aryl halides with phenylboronic acid.

Synthesis, Characterization and Catalytic Utilization of a Ferrocene Diamidodiphosphane

2007 ◽  
Vol 72 (4) ◽  
pp. 453-467 ◽  
Author(s):  
Petr Štěpnička ◽  
Jiří Schulz ◽  
Ivana Císařová ◽  
Karla Fejfarová
Keyword(s):  
Phenylboronic Acid ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Aryl Chlorides ◽  
Highly Active ◽  
Aryl Bromides ◽  
Cross Coupling Reaction

Amidation of 1'-(diphenylphosphanyl)ferrocene-1-carboxylic acid (Hdpf) with ethane-1,2-diamine afforded N,N'-ethylenebis[1'-(diphenylphosphanyl)ferrocene-1-carboxamide] (1), which was isolated in free and solvated form, 1·2AcOH. Both 1 and Hdpf were further converted to their respective phosphane sulfides, 2·2AcOH and 3 that were structurally characterized. Testing of the amidophosphane ligands in Suzuki-Miyaura cross-coupling reaction between phenylboronic acid and various aryl halides revealed that catalyst formed in situ from 1 and palladium(II) acetate is highly active in coupling reactions of aryl bromides whilst the corresponding aryl chlorides showed no or only poor conversions. The catalyst based on 2·2AcOH gave markedly lower yields of the coupling products.

Microwave-promoted Suzuki–Miyaura cross-coupling of aryl halides with phenylboronic acid under aerobic conditions catalyzed by a new palladium complex with a thiosemicarbazone ligand

2006 ◽  
Vol 47 (26) ◽  
pp. 4403-4407 ◽  
Author(s):  
Ioannis D. Kostas ◽  
Georgios A. Heropoulos ◽  
Dimitra Kovala-Demertzi ◽  
Paras N. Yadav ◽  
Jerry P. Jasinski ◽  
...  
Keyword(s):  
Palladium Complex ◽  
Phenylboronic Acid ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Aerobic Conditions ◽  
Thiosemicarbazone Ligand

ChemInform Abstract: Magnetic Fe-Ni Alloy Catalyzed Suzuki Cross-Coupling Reactions of Aryl Halides with Phenylboronic Acid.

ChemInform ◽  
2013 ◽  
Vol 44 (23) ◽  
pp. no-no
Author(s):  
Rongzhao Zhang ◽  
Chengxia Miao ◽  
Shoufeng Wang ◽  
Chungu Xia ◽  
Wei Sun
Keyword(s):  
Phenylboronic Acid ◽  
Cross Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Ni Alloy
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