ScholarWorks@SUNGKYUNKWAN UNIVERSITY: YANG, JUNG WOON

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YANG, JUNG WOON (양정운)

Graduate School (Energy Science)

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Organocatalysis:5||Chiral building block:2||sustainability:2||Enantioselectivity:2||asymmetric catalysis:2||Carboxylic acid:1||Charge transfer:1||Contiguous bisaziridine:1||Contiguous cyclopropylaziridine:1||Cyclic 1,2diketone:1||Cyclopropanation:1||Cyclopropanefused 2chromanone:1||Dicarboxy:1||Domino oxidation:1||Enantioselective:1||EstY29:1||FDCA:1||Fluorine:1||Indanes:1||Ion diffusion:1||Liion battery:1||Michael reaction:1||NHeterocyclic carbene:1||Nitroxide radical:1||Organic battery:1||Oxidative cleavage:1||Oxidative esterification:1||PTMAfilled NCNTs:1||Reaction mechanism:1||Redox active site modification:1||Redox reaction:1||Ringopening reaction:1||Sodium hydride:1||Stereoselective synthesis:1||Substratecontrol:1||Triple cascade reaction:1||Umpolung:1||Voltage tuning:1||acridine:1||biomass:1||borylative coupling:1||catalyst dependence:1||chemoselective:1||chirality:1||contiguous epoxyaziridine:1||copper:1||crystal structure:1||cyclization:1||diastereoselective:1||drug synthesis:1||enantioselective:1||enantioselective epoxidation:1||enantioselectivity:1||esterase:1||fluorides:1||homoallylic alcohol:1||indolines:1||kinetic resolution:1||mixed acetal:1||mukaiyama aldol reaction:1||polyethers:1||rational design:1||regioselective ringopening:1||scaffold diversity:1||stereoconvergent:1||synergistic catalysis:1||terpene biomass:1||transitionmetalfree:1||transitionmetalfree oxidative dehomologation:1||upcycling technology:1||upgrading process:1||ytterbium:1||(S)ketoprofen:1||αBenzylation:1||Asymmetric synthesis:1||Aziridination:1||Caffeine:1||Carbene:1||

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(03063) 25-2, SUNGKYUNKWAN-RO, JONGNO-GU, SEOUL, KOREAsamsunglib@skku.edu

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