교수
이철범 Lee, Chulbom
유기화학 실험실
LAB Website
LAB Website
OFFICE
503-622
/
02-880-6650
LAB
503-602,631
/
02-880-4346
E-MAIL chulbom@snu.ac.kr
RESEARCH AREAS
연구내용
Our program is broadly based on modern organic chemistry (organic synthesis, organometallic chemistry, asymmetric catalysis, natural product total synthesis, bioorganic chemistry). We are developing synthetic tools (reactions and reagents) and networks of reactions (synthetic strategies) for efficient and selective chemical synthesis. In particular, we focus on the development of chemical transformations that can resolve longstanding synthetic problems and offer new mechanistic vistas for future development in organic synthesis. Our investigations are also concerned with the synthesis of natural products with complex molecular architecture and significant biological activities. Our goal is to establish synthetic roadmaps to the target molecules, to evolve new synthesis logics, and to uncover the molecular bases for the peculiar properties of these compounds.
1. New Reaction Development
The research in this area involves discovering, understanding, and exploiting new catalyst systems that effect bond formation with control of chemo-, regio- and stereoselectivities. Our approach is to identify novel reactivities and mechanistic motifs of transition metal-mediated processes to develop conceptually new reactions of broad synthetic utility. Specific topics include the development of stereoselective carbon-heteroatom bond-forming reactions for the asymmetric synthesis of chiral ethers and amines, and new cyclization reactions using alkynes via transition metal vinylidene mediated catalysis.
2. Total Synthesis of Natural Products
Target molecules in our lab include a variety of natural products possessing interesting structural, biological, and physical properties. In each project, we probe the feasibility of unprecedented reactions or untested networks of reactions in complex structural and functional settings. By undertaking these chemical synthesis investigations, we aim to develop innovative new chemistry that will be of great utility in broader contexts. Thus, our endeavor will not only advance synthetic science but also foster opportunities for further biomedical explorations utilizing these molecular agents.
1. New Reaction Development
The research in this area involves discovering, understanding, and exploiting new catalyst systems that effect bond formation with control of chemo-, regio- and stereoselectivities. Our approach is to identify novel reactivities and mechanistic motifs of transition metal-mediated processes to develop conceptually new reactions of broad synthetic utility. Specific topics include the development of stereoselective carbon-heteroatom bond-forming reactions for the asymmetric synthesis of chiral ethers and amines, and new cyclization reactions using alkynes via transition metal vinylidene mediated catalysis.
2. Total Synthesis of Natural Products
Target molecules in our lab include a variety of natural products possessing interesting structural, biological, and physical properties. In each project, we probe the feasibility of unprecedented reactions or untested networks of reactions in complex structural and functional settings. By undertaking these chemical synthesis investigations, we aim to develop innovative new chemistry that will be of great utility in broader contexts. Thus, our endeavor will not only advance synthetic science but also foster opportunities for further biomedical explorations utilizing these molecular agents.
학력
- Ph.D. Chemistry, Stanford University, California, USA, 1998
- BS/MS. Chemistry, Seoul National University 1990
주요 경력
- Associate Professor, Department of Chemistry, Seoul National University, Korea , 2008-Present
- Assistant Professor, Department of Chemistry, Princeton University, New Jersey, USA, 2001-2008
- US Army Cancer Research Postdoctoral Fellow, Memorial Sloan-Kettering Cancer Center, New York, USA, 1999-2001
- Teaching and Research Assistant, Institute for Basic Research, 1991-1992
주요 논문
- “Silyloxymethanesulfinate as a sulfoxylate equivalent for the modular synthesis of sulfones and sulfonyl derivatives,” Dae-Kwon Kim, Hyun-Suk Um, Hoyoon Park, Seonwoo Kim, Jin Choi and Chulbom Lee Chem. Sci. 2020, 11, 13071.
- “Transition Metal Vinylidene- and Allenylidene-Mediated Catalysis in Organic Synthesis,” Sang Weon Roh, Kyoungmin Choi and Chulbom Lee Chem. Rev. 2019, 119, 4293.
- “Rhodium-Catalyzed Tandem Addition–Cyclization–Rearrangement of Alkynylhydrazones with Organoboronic Acids,” Kyoungmin Choi, Hoyoon Park and Chulbom Lee J. Am. Chem. Soc. 2018, 140, 10407.
- “Tandem Diels-Alder and Retro-Ene Reactions of 1-Sulfenyl- and 1-Sulfonyl-1,3-dienes as a Traceless Route to Cyclohexenes,” Jin Choi, Hoyoon Park, Hyun Jung Yoo, Sinae Kim, Erik J. Sorensen, and Chulbom Lee J. Am. Chem. Soc. 2014, 136, 9918.
- “Rhodium-Catalyzed Oxygenative Addiition to Terminal Alkynes for the Synthesis of Esters, Amides and Carboxylic Acids,” Insu Kim and Chulbom Lee Angew. Chem. Int. Ed. 2013, 52, 10023.
- “Visible Light-Induced Photocatalytic Reductive Transformation of Organohalides,” Hyejin Kim and Chulbom Lee Angew. Chem. Int. Ed. 2012, 51, 12303.
논문 검색
39. Synthesis of the C13-C27 Fragment of Madeirolide A Using Visible-Light-Promoted Radical Cyclization
Sunghyun Hwang, Minchul Choi, Myungeun Jeong, Chulbom Lee
Minjung Keum, Dae-Kwon Kim, Hyun-Suk Um, Junsang Lee, chulbom lee
Hyun-Suk Um, Woong Sik Shin, Kyu Jin Son, Chulbom Lee
Dae-Kwon Kim, Minjung Keum, Heekyung Yun, Insu Kim, Jung Min Joo, Chulbom Lee
Dongseok Jang, Minchul Choi, Jinglong Chen, Chulbom Lee
Hyeji Kim, Kyoungmin Choi, Dongseok Jang, Hyun-Suk Um, Yeehwan Kim, Chulbom Lee
Dongseok Jang, Minchul Choi, Jinglong Chen, Chulbom Lee
Yoonjung Cho, Hyeong Jeon An, Taehoon Kim, Chulbom Lee, Nam Ki Lee
Dae-Kwon Kim, Hyun-Suk Um, Hoyoon Park, Seonwoo Kim, Jin Choi, Chulbom Lee
Sang Weon Roh, Kyoungmin Choi, Chulbom Lee