Kee Young Lee
Sungkyunkwan University · Chemistry
About the Lab
Professor Kee Young Lee's research lab specializes in synthetic organic chemistry with a focus on the development of novel catalytic methodologies for the stereoselective synthesis of biologically active natural products and bioactive molecules. The lab employs palladium(0)-catalyzed reactions—particularly oxazoline formation and allylic substitution—for efficient and diastereoselective construction of complex molecular architectures. Additionally, the lab investigates redox signaling pathways and the role of reactive oxygen species in cellular processes, particularly in apoptosis and inflammation, often using model systems such as Chang liver cells. The integration of synthetic methodology with biological evaluation underpins the lab’s interdisciplinary approach to drug discovery and mechanism-based chemical biology.
Research Overview
Research Output Trend
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Selected Papers
15Inositol 1,4,5-trisphosphate (Ins-1,4,5-P3) is an important second-messenger molecule that mobilizes Ca2+ from intracellular stores in response to the occupancy of receptor by various Ca2+-mobilizing agonists. The fate of Ins-1,4,5-P3 is determined by two enzymes, a 3-kinase and a 5-phosphomonoesterase. The first enzyme converts Ins-1,4,5-P3 to Ins-1,3,4,5-P4, whereas the latter forms Ins-1,4-P2. Recent studies suggest that Ins-1,3,4,5-P4 might modulate the entry of Ca2+ from an extracellular so
Selenium is a dietary essential trace nutrient with important biological roles. Selenocompounds were reported to induce apoptosis in many types of tumor cells. In this study, we investigated the signaling pathway involved in the selenite-induced apoptosis using Chang liver cells as a non-malignant cell model. The Chang liver cell apoptosis induced by selenite (10 microM) was confirmed by DNA fragmentation and typical apoptotic nuclear changes. Treatment of selenite increased intracellular reacti
The transformation of acyclic allylic benzamides 4 and homoallylic benzamides 12 to vinyl oxazolines 3 is achieved in the presence of base by the catalysis of Pd(0) in high yield and with high diastereoselectivity. Especially, in the case of homoallylic benzamides 12, trans -oxazolines 3 are formed exclusively or predominantly over cis -oxazolines 8, irrespective of the composition of their stereoisomers. The reaction is believed to proceed via the same π-allylpalladium complex that arises from
Reactive oxygen species (ROS) performs a pivotal function as a signaling mediator in receptor-mediated signaling. However, the sources of ROS in this signaling have yet to be determined, but may include lipoxygenases (LOXs) and NADPH oxidase. The stimulation of lymphoid cells with TNF-α, IL-1β, and LPS resulted in significant ROS production and NF-κB activation. Intriguingly, these responses were markedly abolished via treatment with the LOXs inhibitor nordihydroguaiaretic acid (NDGA). We furthe
[reaction: see text] A concise, stereocontrolled synthesis of sphingofungin F was achieved. Key features involve diastereoselective oxazoline formation catalyzed by palladium(0), MgBr(2)-promoted gamma-alkoxy allylic stannane addition, and palladium(0)-catalyzed coupling of a vinyl iodide with an organozinc reagent.
[structure] The enantioselective total synthesis of (+)-preussin, a potent antifungal agent, has been achieved. The key steps are a Pd(0)-catalyzed oxazoline-forming reaction from L-phenylalanine, hydrogenolysis, and subsequent diastereoselective reductive cyclization of the intermediate aminoketone to pyrrolidine using Pearlman's catalyst.
We report a new asymmetric synthetic method for (-)-swainsonine utilizing a chiral oxazoline precursor. The key features in this strategy are the diastereoselective oxazoline formation reaction catalyzed by palladium(0), diasteroselective dihydroxylation, and the stereocontrolled allylation reaction with TiCl(4).
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In this paper, we apply the concept of the group \ulcorner(X,A) of self pair homotopy equivalences of a CW-pair (X, A) to the Postnikov system. By using a short exact sequence related to the group of self pair homotopy equivalences, we obtain the following result: for any Postnikov section Xn/ of a CW-complex X, the group \ulcorner(Xn/, A) of self pair homotopy equivalences on the pair (Xn/, X) is isomorphic to the group \ulcorner(X) of self homotopy equivalences on X. As a corollary, we have, \
Purpose: This study aimed to compare short-term postoperative and oncologic outcomes of a transanal endoscopic total mesorectal excision (TME) to those of a transabdominal robotic TME. Methods: A total of 62 patients with rectal cancer underwent transanal (n = 26) or robotic (n = 36) TME between June 2013 and December 2014. After case-matching by tumor location and TNM stage, 45 patients were included for analysis. The median follow-up period was 21.3 months. Operative, histopathologic and posto
This paper observes that the induced homomorphisms on cohomology groups by a cyclic map are trivial. For a CW-complex X, we use the fact to obtain some conditions of X so that the n-th Gottlieb group <TEX>$G_n(X)$</TEX> is trivial for an even positive integer n. As corollaries, for any positive integer m, we obtain <TEX>$G_{2m}(S^{2m})\;=\;0\;and\;G_2(CP^m)\;=\;0$</TEX> which are due to D. H. Gottlieb and G. Lang respectively, where <TEX>$S^{2m}$</TEX> is the 2m- dimensional sphere and <TEX>$CP^
Research Areas
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