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Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile
Published on: October 30, 2018
Contra-Thermodynamic Chain-Walking Isomerization: A Sustainable Tool for Selective Molecular Editing in Green
Gábor Turczel1,2, Ádám Erdélyi1,2, Márton Nagyházi1,2
1Institute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, Budapest, Hungary.
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Contra-thermodynamic chain-walking isomerization has emerged as a powerful strategy in green chemistry for the selective transformation of alkenes and functionalized hydrocarbons under relatively mild (typically below 100°C) conditions. Unlike conventional thermodynamically driven isomerizations that favor the most stable olefin products, contra-thermodynamic processes enable the migration of double bonds toward less stable, yet more synthetically valuable positions. This directional control allows access to otherwise difficult-to-obtain isomers without the need for pre-functionalized substrates or multistep synthesis. By employing tailored, selective transition-metal catalysts, light-driven systems, or redox-mediated pathways, contra-thermodynamic chain-walking can proceed with high atom economy and minimal waste generation. Moreover, this methodology enables even the late-stage functionalization and valorization of biomass-derived feedstocks. Continued development of more efficient and recyclable catalytic systems is expected to further expand the environmental and industrial relevance of contra-thermodynamic chain-walking isomerization.
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