Melting process of nanoparticle enhanced PCM through storage cylinder incorporating fins

Approaches for expedition of discharging of PCM involving nanoparticles and radial fins

Electrochemical multicomponent synthesis of 4-selanylpyrazoles under catalyst- and chemical-oxidant-free conditions

Nanoparticles for phase change process of water utilizing FEM

Heat recovery application of nanomaterial with existence of turbulator

Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade

The study reported an electrochemically mediated method for the preparation of 2,1-benzoxazoles from o-nitrophenylacetylenes. Different from the traditional electrochemical reduction of nitro to ni...

Electrochemically Enabled Selenium Catalytic Synthesis of 2,1-Benzoxazoles from o-Nitrophenylacetylenes.

Azoles and organoselenium compounds are pharmacologically important scaffolds in medicinal chemistry and natural products. We developed an efficient regioselective electrochemical aminoselenation reaction of 1,3-dienes, azoles, and diselenide derivatives to access selenium-containing allylazoles skeletons. This protocol is more economical and environmentally friendly and features a broad substrate scope; pyrazole, triazole, and tetrazolium were all tolerated under the standard conditions, which could be applied to the expedient synthesis of bioactive molecules and in the pharmaceutical industry.

Lin-Wei Wang

Papers

Electrochemically enabled synthesis of sulfide imidazopyridines via a radical cyclization cascade

Electrochemically Enabled Selenium Catalytic Synthesis of 2,1-Benzoxazoles from o-Nitrophenylacetylenes.

Three-Component Electrochemical Aminoselenation of 1,3-Dienes.