Copper oxidecatalysts have been prepared by pyrolysis of copper acetate on aluminum oxide. The material resulting from pyrolysis at 800 °C allows for catalytic hydrogenations at low temperature of a variety of unsaturated compounds such as quinolines, alkynes, ketones, imines, and polycyclic aromatic hydrocarbons as well as nitroarenes with good activity and selectivity.
Copper- and phosphine-free Sonogashira coupling reactions of aryl iodides catalyzed by an N,N-bis(naphthylideneimino)diethylenetriamine-functionalized polystyrene resin supported Pd(II) complex under aerobic conditions
作者:Mohammad Bakherad、Amir H. Amin、Ali Keivanloo、Bahram Bahramian、Mersad Raeissi
DOI:10.1016/j.tetlet.2010.07.011
日期:2010.10
A polymer-supported palladium(II) N,N-bis(naphthylideneimino)diethylenetriamine complex is found to be a highly active catalyst for Sonogashira coupling reactions. The reactions are performed under copper- and phosphine-free conditions in an air atmosphere. The palladium catalyst is easily separated, and can be reused several times without significant loss in catalytic activity.
Monodisperse nickel-nanoparticles for stereo- and chemoselective hydrogenation of alkynes to alkenes
作者:Kathiravan Murugesan、Ahmad S. Alshammari、Manzar Sohail、Matthias Beller、Rajenahally V. Jagadeesh
DOI:10.1016/j.jcat.2018.12.018
日期:2019.2
Here, we report the use of monosaccharides for the preparation of novel nickel nanoparticles (NP), which constitute selective hydrogenation catalysts. For example, immobilization of fructose and Ni(OAc)2 on silica and subsequent pyrolysis under inert atmosphere produced graphitic shells encapsulated Ni-NP with uniform size and distribution. Interestingly, fructose acts as structure controlling compound
Simple and efficient nickel-catalyzed cross-coupling reaction of alkynylalanes with benzylic and aryl bromides
作者:Deepak B. Biradar、Han-Mou Gau
DOI:10.1039/c1cc14206b
日期:——
efficient and simple coupling reactions of benzylic and arylbromides with aluminium acetylide catalyzed by NiCl(2)(PPh(3))(2) are reported. The coupling reactions proceed at room temperature employing 4 mol% catalyst, affording coupling products in excellent yields of up to 95% in short reaction times. The system worked efficiently with aryl and heterocyclic bromides as well.