Organic electrosynthesis is a green strategy for the synthesis of valuable molecules.
Electrochemical reactions using sacrificial metal anodes enable new reactivity to be …

Compared with general redox chemistry, electrochemistry using the electron as a potent,
controllable, yet traceless alternative to chemical oxidants/reductants usually offers more …

The cross-electrophile dialkylation of alkenes enables the formation of two C (sp3)–C (sp3)
bonds from readily available starting materials in a single transformation, thereby providing …

Herein, an efficient and facile approach to valuable β‐hydroxy acid derivatives from readily
available aryl epoxides and CO2 with high chemo‐and regioselectivity under mild and …

Herein, an electroreductive carboxylation of organic carbon‐halogen bonds (X= Br and Cl)
promoted by catalytic amounts of naphthalene as an organic mediator is reported. This …

We present a new, unified approach for the transformation of benzylic and allylic alcohols,
aldehydes, and ketones into boronic esters under electroreductive conditions. Key to our …

Formation of new C (sp3)–C (sp3) bonds is a powerful synthetic tool to increase molecular
diversity, which is highly sought after in medicinal chemistry. Traditional generation of …

The development of general and selective methods to generate and transform reactive
intermediates such as radicals, cations, and anions remains an important objective in …

Electron‐deficient acridones and in situ generated acridinium salts are reported as potent,
closed‐shell photooxidants that undergo surprising mechanisms. When bridging acyclic …

The formation of C (sp3)–C (sp3) and C (sp3)–C (sp2) bonds is one of the major research
goals of synthetic chemists. Electrochemistry is commonly considered to be an appealing …