Recoverable PEG-Supported Copper Catalyst for Highly Stereocontrolled Nitroaldol Condensation.

Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes.

Remarkable generality in scope of DATs/Cu catalysts for enantioselective nitroaldol reaction is described; excellent levels of stereoinduction are recorded for a range of aldehydes (ee 81-99%, 17 examples) and the possibility to employ the present catalytic system as the key step for the preparation of highly functionalized tetrahydro-isoquinolines is demonstrated.

Mn (III) salen complex supported on graphene oxide nanosheets as a highly selective and recoverable catalyst for the oxidation of sulfides

In this study, Mn (III) salen complex was synthesized and immobilized onto the graphene oxide, which is modified by 3-chloropropyltrimethoxy silane. Heterogeneous catalyst was characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, fourier transform infrared spectra, nitrogen adsorption−desorption isotherm and atomic absorption spectroscopy. The catalyt...

Novel carbohydrate-derived prolinamide as a highly efficient, recoverable catalyst for direct aldol reactions in water

Reductive Ullmann Coupling of Aryl Halides by Palladium Nanoparticles Supported on Cellulose, a Recoverable Heterogeneous Catalyst

Palladium nanoparticles supported on cellulose were prepared without using any reducing agent and used as a highly efficient catalyst for the Ullmann reductive coupling of aryl halides in the presence of zinc, in a water-alcohol mixture as solvent in air. The obtained palladium nanoparticles were characterized by scanning electron microscopy (SEM), FTIR, thermogravimetric analysis (TGA) and ICP...

Graphene-supported hemin as a highly active biomimetic oxidation catalyst.

Well supported: stable hemin-graphene conjugates formed by immobilization of monomeric hemin on graphene, showed excellent catalytic activity, more than 10 times better than that of the recently developed hemin-hydrogel system and 100 times better than that of unsupported hemin. The catalysts also showed excellent binding affinities and catalytic efficiencies approaching that of natural enzymes.