An efficient electrochemical protocol for the synthesis of α-amino ketones via the oxidative cross-dehydrogenative coupling of ketones and secondary amines has been developed. The electrochemistry performs in a simple undivided cell using NH<sub>4</sub>I as a redox catalyst and a cheap graphite plate as electrodes under constant current conditions. Gram-scale reaction demonstrates the practicality of the protocol. The reaction is proposed to procced through an initial α-iodination of ketone, followed by a nucleophilic substitution of amines
Electrochemical oxidation represents an environmentally friendly solution to conventional methods th...
Abstract Direct functionalization of C(sp3)–H bonds allows rapid access to valuable products, starti...
Disubstituted malonic acid derivatives are smoothly converted into diketones and ketoesters in good ...
The multifunctionalization of unactivated cyclic ketones was developed via an electrochemically inte...
Herein, we report an efficient electrochemical activation of the C–C bond of aryl ketones for the pr...
The significance of α-functionalization of carbonyl compounds arises from its frequent use in synthe...
A transition-metal-free direct α-C–H amination of ketones has been developed using commercially avai...
The electrochemically induced cross-dehydrogenative C–O coupling of β-diketones and β-ketoesters (C–...
A novel electrochemical oxidative decarboxylation of disubstituted malonic acids leading to dimethox...
A novel electrochemical oxidative decarboxylation of disubstituted malonic acids leading to dimethox...
An electrochemically intramolecular functionalization of C(sp<sup>3</sup>)–H bonds with masked oxyg...
The cross-coupling of C(sp3)–H and N–H represents one of the most straightforward approaches to con...
This thesis describes the exploration and development of electrochemical methods for the generatio...
The multistep synthesis of natural products has historically served as a useful and informative plat...
α-Pyridyl tertiary amino acids have potential pharmaceutical applications because of their structura...
Electrochemical oxidation represents an environmentally friendly solution to conventional methods th...
Abstract Direct functionalization of C(sp3)–H bonds allows rapid access to valuable products, starti...
Disubstituted malonic acid derivatives are smoothly converted into diketones and ketoesters in good ...
The multifunctionalization of unactivated cyclic ketones was developed via an electrochemically inte...
Herein, we report an efficient electrochemical activation of the C–C bond of aryl ketones for the pr...
The significance of α-functionalization of carbonyl compounds arises from its frequent use in synthe...
A transition-metal-free direct α-C–H amination of ketones has been developed using commercially avai...
The electrochemically induced cross-dehydrogenative C–O coupling of β-diketones and β-ketoesters (C–...
A novel electrochemical oxidative decarboxylation of disubstituted malonic acids leading to dimethox...
A novel electrochemical oxidative decarboxylation of disubstituted malonic acids leading to dimethox...
An electrochemically intramolecular functionalization of C(sp<sup>3</sup>)–H bonds with masked oxyg...
The cross-coupling of C(sp3)–H and N–H represents one of the most straightforward approaches to con...
This thesis describes the exploration and development of electrochemical methods for the generatio...
The multistep synthesis of natural products has historically served as a useful and informative plat...
α-Pyridyl tertiary amino acids have potential pharmaceutical applications because of their structura...
Electrochemical oxidation represents an environmentally friendly solution to conventional methods th...
Abstract Direct functionalization of C(sp3)–H bonds allows rapid access to valuable products, starti...
Disubstituted malonic acid derivatives are smoothly converted into diketones and ketoesters in good ...