A simple high-yielding method for the preparation of a tetramethylcyclopentadienyl-NHC ligand is described. This ligand has been successfully coordinated to Rh and Ir. A related Cp*-NHC ligand with a -CH(2)CMePh- linker between the Cp* and the NHC is also described, together with its coordination to Rh and Ir. This latter ligand, affords the orthocyclometallation of the phenyl ring yielding a c...

Plants are subject to a wide range of abiotic stresses, and their cuticular wax layer provides a protective barrier, which consists predominantly of long-chain hydrocarbon compounds, including alkanes, primary alcohols, aldehydes, secondary alcohols, ketones, esters and other derived compounds. This article discusses current knowledge relating to the effects of stress on cuticular waxes and the...

A mild, iron-based catalyst system is presented that selectively oxidizes secondary alcohols to the corresponding hydroxy ketones in the presence of primary alcohols within 15 minutes at room temperature, utilizing H2O2 as the oxidant.

Reversibility of a dehydrogenation/hydrogenation catalytic reaction has been an elusive target for homogeneous catalysis. In this report, reversible acceptorless dehydrogenation of secondary alcohols and diols on iron pincer complexes and reversible oxidative dehydrogenation of primary alcohols/reduction of aldehydes with separate transfer of protons and electrons on iridium complexes are shown...

Urea, the white gold: The efficient synthesis of tertiary and secondary amines is achieved by heterogeneous gold-catalyzed direct amination of stoichiometric alcohols with urea in good to excellent yields. Via a hydrogen autotransfer pathway, the reactions of primary alcohols with urea give tertiary amines exclusively, while secondary alcohols selectively afford secondary amines.

nanomagnetic mgfe2o4 is an active, stable, and reusable catalyst for the oxidation of alcohols. the oxidation of various primary and secondary alcohols has been examined and related corresponding products were obtained in good yields. the reactions were carried out in the presence of water as solvent and oxone (at room temperature) or h2o2 (at 60 ºc) as an oxidant. the catalyst was investigated...

The regio- and chemoselective oxidation of unprotected vicinal polyols with [(neocuproine)Pd(OAc)]2(OTf)2 (1) (neocuproine = 2,9-dimethyl-1,10-phenanthroline) occurs readily under mild reaction conditions to generate α-hydroxy ketones. The oxidation of vicinal diols is both faster and more selective than the oxidation of primary and secondary alcohols; vicinal 1,2-diols are oxidized selectively...

Nanomagnetic NiFe2O4 was used as the efficient, stable, reusable catalyst for selective oxidation of alcohols to their corresponding carbonyl compounds using oxone (potassium hydrogen monopersulfate) as oxidant in the presence of water as solvent at room temperature. The oxidation of various primary and secondary alcohols has been examined and related corresponding products were obtained wi...

Nanomagnetic MgFe2O4 is an active, stable, and reusable catalyst for the oxidation of alcohols. The oxidation of various primary and secondary alcohols has been examined and related corresponding products were obtained in good yields. The reactions were carried out in the presence of water as solvent and oxone (at room temperature) or H2O2 (at 60 ºC) as an oxidant. The catalyst was investigated...

an efficient protocol for the selective oxidation of primary alcohols to aldehydes withh5io6/v2o5 in ionic liquid [bmpy][pf6] has been developed. high yields of the products, mildreaction conditions and simple experimental procedure make this protocol complementary tothe existing methods. the catalyst can be reused for several times without obvious loss of thecatalytic activity.