当前位置: X-MOL首页全球导师 海外导师 › Kwon, Ohyun
扫描左侧二维码
使用公众号菜单
手机上轻松查询100,000+导师

个人简介

Ohyun Kwon received her B.S. (1991) and M.S. (1993) from Seoul National University in South Korea. In 1993, she came to the U.S. to pursue her Ph.D. (1998) from Columbia University under the guidance of S. J. Danishefsky. Her thesis work involved the synthesis of biologically significant glycolipid, asialo GM1 and Globo-H human breast tumor antigen molecule, as well as complex phomoidride terpenoids, CP-225,917 and CP-263,114. She then went to Harvard University as a Howard Hughes Postdoctoral Fellow to study chemical genetics in S. L. Schreiber's lab. There, she completed a diversity-oriented combinatorial synthesis (DOS) of a library of muticyclic compounds, as well as a library of macrocycles. Kwon joined the faculty as an assistant professor at UCLA in 2001. She has been a member of the Molecular Biology Institute (MBI) and UCLA Jonsson Comprehensive Cancer Center (JCCC) since 2005. Her research at UCLA evolves around the development of new nucleophilic phosphine catalysis reactions. The new reaction methodologies are used in the total synthesis of natural products and in the production of libraies of small organic molecules for chemical genetic applications.

研究领域

organic/Chemical Biology/Synthesis

Our research interest lies in the area of development of new methodologies for organic transformations, target oriented synthesis of biologically important natural compounds, and diversity oriented synthesis of natural product-like molecules. Molecules thus built will be employed in the investigation of biologically significant processes. Each project described below encompasses more than one area of these research interests.

近期论文

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

Lu, J.; Chan, L.; Fiji, H. D. G.; Dahl, R.; Kwon, O.; Tamanoi, F In vivo anticancer effect of a novel inhibitor of protein geranylgeranyltransferase I, Mol. Cancer Ther., 2009; 8: 1218-1226. Guo, H.; Xu, Q.; Kwon, O. Phosphine-Promoted [3+3] Annulation of Aziridines with Allenoates: A Facile Entry into Highly Functionalized Tetrahydropyridines, J. Am. Chem. Soc, 2009; 131: 6318-6319. Lu, K.; Kwon, O Phosphine-catalyzed [4+2] Annulation: Synthesis of Ethyl 6-phenyl-1-tosyl-1,2,5,6-tetrahydropyridine-3-carboxylate Org. Synth, 2009; 86: 212-224. Creech, G. S.; Kwon, O. Alcohol-Assisted Phosphine Catalysis: One-Step Synthesis of Dihydropyrone from Aldehyde and Allenoate, Org. Lett., 2008; 10: 429?432. Andrews, I.P., Kwon, O. Highly Efficient Palladium-Catalyzed Hydrostannation of Ethyl Ethynyl Ether Tetrahedron Lett., 2008; 49: 7097-7099. Watanabe, M.; Fiji, H. D. G.; Guo, L.; Umetsu, A.; Kinderman, S. S.; Slamon, D. J.; Kwon, O.; Tamanoi, F. Inhibitors of protein geranylgeranyltransferase-I and Rab geranylgeranyltransferase identified from a library of allenoate derived compounds, J. Biol. Chem., 2008; 283: 9571?9579. Creech, G. S.; Zhu, X.; Fonovic, B.; Dudding, T.; Kwon, O. Theory-Guided Design of Brønsted Acid-Assisted Phosphine Catalysis: Synthesis of Dihydropyrones from Aldehydes and Allenoates, Tetrahedron, 2008; 64: 6935?6942. Sriramurthy, V.; Barcan, G. A.; Kwon, O. Bisphosphine-Catalyzed Mixed Double-Michael Reactions: Asymmetric Synthesis of Oxazolidines, Thiazolidines, and Pyrrolidines, J. Am. Chem. Soc., 2007; 129: 12928?12929 (Highlighted in SYNFACTS 2008, 19; Featured as a Synstory in SYNFORM 2008, A10?A12).

推荐链接
down
wechat
bug