- * 프린트는 Chrome에 최적화 되어있습니다. print
The major research themes in our laboratory are to develop metal-catalyzed synthetic routes to afford functionalized small molecules. Issues of regiochemistry, oxidation state changes of transition metal complexes, and efficiency to construct carbon–carbon and carbon–heteroatoms have been the central topics of our synthetic approaches.
Major research field
유기합성, 레독스 반응, 전이금속 촉매 반응
Desired field of research
Research Keywords and Topics
The SYH group’s research centers on selective bond activation and functionalization for molecular complexity. Our research themes include (i) metal-catalyzed selective transformations and/or functionalizations of π-system, (ii) directed or nondirected C−H arylation of (hetero)arenes using hypervalent compounds, and (iii) oxidation-state modulation to access active radical species or to activate inert bonds.
Research Publications
MORE- Nat. Commun. 2022, 13, 2421. "Rapid access to polycyclic N-heteroarenes from unactivated, simple azines via a base-promoted Minisci-type annulation" Lee, J. B.; Kim, G. H.; Jeon, J. H.; Jeong, S. Y.; Lee, S.; Park, J.; Lee, D.; Kwon, Y.; Seo, J. K.; Chun, J.-H.; Kang, S. J.; Choe, W.; Rohde, J.-U.*; Hong, S. Y.*
- J. Am. Chem. Soc. 2017, 139, 12121–12124. “Nickel-catalyzed azide–alkyne cycloaddition to access 1,5-disubstituted 1,2,3-triazoles in air and water” Kim, W. G.; Kang, M. E.; Lee, J. B.; Jeon, M. H.; Lee, S.; Lee, J.; Choi, B.; Cal, P. M. S. D.; Kang, S.; Kee, J.-M.; Bernardes, G. J. L.; Rohde, J.-U.; Choe, W.; Hong, S. Y.*
- Angew. Chem., Int. Ed. 2017, 56, 5007–5011. “An annulative synthetic strategy for building triphenylene frameworks via multiple C–H activations” Mathew, B. P. ‡; Yang, H. J.‡; Kim, J.; Lee, J. B.; Kim, Y.-T.; Lee, S.; Lee, C. Y.; Choe, W.; Myung, K.; Park, J.-U.*; Hong, S. Y.**
국가과학기술표준분류
- NC. 화학
- NC02. 유기화학
- NC0203. 유기합성방법론
국가기술지도분류
- 환경/에너지 프론티어 진흥
- 031900. 2차 전지기술
녹색기술분류
- 고효율화기술
- 친환경 제조공정 및 소재효율성 향상
- 352. 제조공정/소재 효율성 향상 기타 기술
6T분류
- ET 분야
- 에너지
- 050211. 에너지소재기술