ChemInform Abstract: High Yield Olefination of a Wide Scope of Aryl Chlorides Catalyzed by the Phosphinito Palladium PCP Pincer Complex: [PdCl{C6H3(O-P(iPr)2)2-2,6}].

ChemInform ◽  
2000 ◽  
Vol 31 (48) ◽  
pp. no-no
Author(s):  
David Morales-Morales ◽  
Rocio Redon ◽  
Cathleen Yung ◽  
Craig M. Jensen

2000 ◽  
pp. 1619-1620 ◽  
Author(s):  
David Morales-Morales ◽  
Rocío Redón ◽  
Cathleen Yung ◽  
Craig M. Jensen


2006 ◽  
Vol 47 (29) ◽  
pp. 5059-5062 ◽  
Author(s):  
Valente Gómez-Benítez ◽  
Oscar Baldovino-Pantaleón ◽  
Cesar Herrera-Álvarez ◽  
Rubén A. Toscano ◽  
David Morales-Morales
Keyword(s):  


2018 ◽  
Vol 37 (20) ◽  
pp. 3475-3479 ◽  
Author(s):  
Daniel Himmelbauer ◽  
Berthold Stöger ◽  
Luis F. Veiros ◽  
Karl Kirchner
Keyword(s):  


Molecules ◽  
2019 ◽  
Vol 24 (12) ◽  
pp. 2296 ◽  
Author(s):  
Toru Hashimoto ◽  
Kei Funatsu ◽  
Atsufumi Ohtani ◽  
Erika Asano ◽  
Yoshitaka Yamaguchi

A cross-coupling reaction of allylic aryl ethers with arylmagnesium reagents was investigated using β-aminoketonato- and β-diketiminato-based pincer-type nickel(II) complexes as catalysts. An β-aminoketonato nickel(II) complex bearing a diphenylphosphino group as a third donor effectively catalyzed the reaction to afford the target cross-coupled products, allylbenzene derivatives, in high yield. The regioselective reaction of a variety of substituted cinnamyl ethers proceeded to give the corresponding linear products. In contrast, α- and γ-alkyl substituted allylic ethers afforded a mixture of the linear and branched products. These results indicated that the coupling reaction proceeded via a π-allyl nickel intermediate.



2014 ◽  
Vol 43 (32) ◽  
pp. 12187-12199 ◽  
Author(s):  
Wolfgang Leis ◽  
Sophie Wernitz ◽  
Benedikt Reichart ◽  
David Ruckerbauer ◽  
Johannes Wolfram Wielandt ◽  
...  

Chemical conversions of a cycloheptatriene iridium pincer complex were studied by NMR and MS techniques as well as DFT calculations.



2002 ◽  
Vol 189 (1) ◽  
pp. 119-124 ◽  
Author(s):  
Xue-Qin Gu ◽  
Wei Chen ◽  
David Morales-Morales ◽  
Craig M. Jensen


2015 ◽  
Vol 51 (10) ◽  
pp. 1897-1900 ◽  
Author(s):  
Eva Jürgens ◽  
Barbara Wucher ◽  
Frank Rominger ◽  
Karl W. Törnroos ◽  
Doris Kunz

The highly nucleophilic complex 1 isomerises terminal epoxides exclusively to the respective methylketones in very high yield under mild conditions.



Synthesis ◽  
2019 ◽  
Vol 51 (24) ◽  
pp. 4590-4600
Author(s):  
Yuanguang Chen ◽  
Fangyu Du ◽  
Fengyang Chen ◽  
Qifan Zhou ◽  
Guoliang Chen

In the selective N-arylation of amines or azoles with aryl halides­, methyl-α-d-glucopyranoside (MG) was found to function as a green ligand of copper powder. In addition, nitrogen heterocyclic amine compounds can also undergo the N-arylation coupling with heterocyclic aryl chlorides. This process allows access to a variety of aromatic amines and aryl azoles under mild reaction conditions, has good tolerance, and proceeds in moderate to high yield.



Synthesis ◽  
2019 ◽  
Vol 51 (20) ◽  
pp. 3792-3795 ◽  
Author(s):  
Yuya Ashida ◽  
Shoichi Kondo ◽  
Kazuya Arashiba ◽  
Takamasa Kikuchi ◽  
Kazunari Nakajima ◽  
...  

A practical method for ammonia synthesis is described. The reaction of atmospheric pressure of nitrogen gas with samarium diiodide as a reducing reagent and water as a proton source in the presence of a catalytic amount of a molybdenum trichloride complex bearing a PCP [1,3-bis(di-tert-butylphosphinomethyl)benzimidazol-2-ylidene]-type pincer ligand occurs under ambient conditions to afford ammonium sulfate after treatment with sulfuric acid.



Polyhedron ◽  
2007 ◽  
Vol 26 (7) ◽  
pp. 1445-1448 ◽  
Author(s):  
Ali Naghipour ◽  
S.J. Sabounchei ◽  
David Morales-Morales ◽  
Daniel Canseco-González ◽  
Craig M. Jensen


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