Dong Il Park

ORCID: 0000-0003-4410-8972
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About
Contact & Profiles
Research Areas
  • Radical Photochemical Reactions
  • Electrochemical Analysis and Applications
  • Copper Interconnects and Reliability
  • Synthesis and Characterization of Heterocyclic Compounds
  • Synthesis and Catalytic Reactions
  • Synthesis of heterocyclic compounds
  • Multicomponent Synthesis of Heterocycles
  • Advanced Thermoelectric Materials and Devices
  • Thermal properties of materials
  • Catalytic C–H Functionalization Methods
  • Molecular Junctions and Nanostructures
  • Metal and Thin Film Mechanics
  • Ionic liquids properties and applications
  • Electrocatalysts for Energy Conversion
  • CO2 Reduction Techniques and Catalysts
  • Ammonia Synthesis and Nitrogen Reduction
  • Semiconductor materials and devices

Korea University
2020-2023

University of Chicago
2023

Sun Moon University
1997

Nitrogen scanning in aryl fragments is a valuable aspect of the drug discovery process, but current strategies require time-intensive, parallel, bottom-up synthesis each pyridyl isomer because lack direct carbon-to-nitrogen (C-to-N) replacement reactions. We report site-directable C-to-N reaction allowing unified access to various pyridine isomers through nitrene-internalization process. In two-step, one-pot procedure, azides are first photochemically converted 3

10.1126/science.adj5331 article EN Science 2023-09-28

Recent advances in the physicochemical understanding of thermal transport across molecular junctions single molecules and monolayers are discussed.

10.1039/d0ta07095e article EN Journal of Materials Chemistry A 2020-01-01

Reductive amination has been widely used for manufacturing carbon-nitrogen-containing building blocks. Despite its versatility, the need a chemical reductant or harmful hydrogen gas limited further utilization in modern applications. Here, we report electrochemical reductive (ERA) to pursue sustainable synthetic routes. Faradaic efficiencies of about 83% are achieved using Cu metal electrodes. In-depth electrokinetic studies reveal rate-determining step and overall reaction nature ERA....

10.1039/d3cc00296a article EN Chemical Communications 2023-01-01

A four-step synthesis of trisubstituted pyridines from Baylis-Hillman adducts 1 is reported. The SN2′ reaction products 2 are subjected to combined Michael addition-aldol condensation give 3 which, upon treatment with Cs2CO3, pyridine derivatives 4. scope and limitations this procedure were not widely investigated.

10.1055/s-2006-934502 article EN Synfacts 2006-05-19
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