Results 151 to 160 of about 131,045 (252)
Design and Biological Evaluation of Palladium(II)-Phosphine-Benzimidazole Complexes as Dual Antioxidant and Antiangiogenic Agents. [PDF]
Kiyan HT +4 more
europepmc +1 more source
Recent Developments in the Field of Air‐Stable Nickel(0) Precatalysts for Cross‐Coupling Reactions
The development of bench‐stable Ni(0) sources aims to replace air‐sensitive [Ni(COD)2] (cod = cycloocta‐1,5‐diene) with easy‐to‐handle alternatives. Through a targeted ligand design, using electron‐deficient dienes, carbenes, and fluorophosphines, researchers have achieved air‐ and moisture‐tolerant complexes that show high catalytic activity in cross ...
Franziska Flecken, Schirin Hanf
wiley +1 more source
Application of statistical design of experiment to identify key factors in cross coupling reactions. [PDF]
Radzilani F, Zinyemba O, Meijboom R.
europepmc +1 more source
Rigid Ligand Environments at Beryllium, From Spectroscopic Probes to Small Molecule Activation
Due to the high rigidity and definition of beryllium scorpionate complexes, they can be used to study metal‐pseudohalide and ‐carbon bonds in detail. Furthermore, these compounds can be used to activate small molecules and exhibit unprecedented transmetalation reactions. In beryllium scorpionate complexes, three of the four available coordination sites
Magnus R. Buchner, Chantsalmaa Berthold
wiley +1 more source
Evaluating the Antiproliferative Effects of Tri(2-Furyl)- and Triphenylphosphine-Gold(I) Pyridyl- and Pyrimidine-Thiolate Complexes. [PDF]
Wilhelm KL +11 more
europepmc +1 more source
An improved synthesis of a manganese catalyst used for hydrogenation of ketones, esters and imines is reported. The catalyst has now been found to effect tandem conjugate reduction‐ester hydrogenations with very low amounts of allylic alcohol by‐products.
José A. Fuentes, Matthew L. Clarke
wiley +1 more source
Mechanistically Driven Development of Kumada Catalyst-Transfer Polymerizations: A Rapid Injection NMR Study. [PDF]
Kang S +7 more
europepmc +1 more source
We report a carbonylation‐homolysis process to access acyl radicals that can undergo decarboxylation or cyclization onto tethered alkenes. In both cases, ligands and additives are shown to influence the outcome to give saturated or unsaturated products, in some cases with isomerization of the initial products.
Jacob N. Hackbarth +4 more
wiley +1 more source

