Add to ORKGA mild molybdenum-catalyzed, aerobic, chemoselective oxidation of benzylic azides to the corresponding aldehydes in an aqueous medium that tolerates a variety of functional groups including alcohols, esters,ketones, halides and olefins is described
Herein, we present a study on the oxidation of aldehydes to carboxylic acids using three recombinant...
A novel procedure for the catalytic aerobic oxidation of alcohols into carbonyl derivatives under ne...
Abstract: The oxidation of benzylic alcohols is a ubiquitous transformation in organic chemistry due...
Csp3⁻H oxidation of benzylic methylene compounds is an established strategy for the synthesis ...
A chemoselective, neutral, and efficient strategy for the reduction of azides to corresponding ami...
Whilst allowing for easy access to synthetically versatile motifs and for modification of bioactive ...
A highly efficient catalytic system without transition metals in water has been developed for aerobi...
We reported herein new reactivities and possible mechanistic implications of a simplest oxidant (NaH...
Efficient aerobic oxidation of benzylic Compounds has been achieved under no irradiation using a new...
A unique combination of a supported cobalt complex and the first example of supported NHPI in acetic...
A general strategy involving a novel and highly efficient aerobic benzylic oxidation promoted by che...
The chemoselective oxidation of alcohols containing electron-rich sulfur functionalities (e.g., 1,3-...
Oxidation of alcohols to aldehydes and ketones has been studied in high yields using molecular oxyge...
Aerobic alcohol oxidation using a PdCl2/N,N-dimethylacetamide catalyst system under mild condition
The first example organocatalyzed aerobic oxidation of aldehydes to carboxylic acids in both organic...
Herein, we present a study on the oxidation of aldehydes to carboxylic acids using three recombinant...
A novel procedure for the catalytic aerobic oxidation of alcohols into carbonyl derivatives under ne...
Abstract: The oxidation of benzylic alcohols is a ubiquitous transformation in organic chemistry due...
Csp3⁻H oxidation of benzylic methylene compounds is an established strategy for the synthesis ...
A chemoselective, neutral, and efficient strategy for the reduction of azides to corresponding ami...
Whilst allowing for easy access to synthetically versatile motifs and for modification of bioactive ...
A highly efficient catalytic system without transition metals in water has been developed for aerobi...
We reported herein new reactivities and possible mechanistic implications of a simplest oxidant (NaH...
Efficient aerobic oxidation of benzylic Compounds has been achieved under no irradiation using a new...
A unique combination of a supported cobalt complex and the first example of supported NHPI in acetic...
A general strategy involving a novel and highly efficient aerobic benzylic oxidation promoted by che...
The chemoselective oxidation of alcohols containing electron-rich sulfur functionalities (e.g., 1,3-...
Oxidation of alcohols to aldehydes and ketones has been studied in high yields using molecular oxyge...
Aerobic alcohol oxidation using a PdCl2/N,N-dimethylacetamide catalyst system under mild condition
The first example organocatalyzed aerobic oxidation of aldehydes to carboxylic acids in both organic...
Herein, we present a study on the oxidation of aldehydes to carboxylic acids using three recombinant...
A novel procedure for the catalytic aerobic oxidation of alcohols into carbonyl derivatives under ne...
Abstract: The oxidation of benzylic alcohols is a ubiquitous transformation in organic chemistry due...