정병혁
Jung, ByunghyuckDepartment of Physics and Chemistry
학력
- 2004 ~ 2008한국과학기술원 박사
- 2002 ~ 2004한국과학기술원 석사
- 1998 ~ 2002한국과학기술원 학사
경력
- 2014 ~ CurrentDGIST, 기초학부 / 조교수
- 2010 ~ 2013Boston College / 박사후연구원
- 2009 ~ 2010KAIST / 연수연구원
- 2008 ~ 2009삼성전기 / 책임연구원
수상실적
- 2023총장표창
연구실 소개
- Asymmetric Organic Synthesis and Drug Synthesis Laboratory
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Most of drugs, including Remdesivir® as a potential candidate for COVID-19, have chiral carbon-centers and Thalidomide-scandal had brought the importance of stereoselective synthesis of drugs. In this sense, we pursue the development of practical and efficient asymmetric reactions to apply for the lab-scale or bulk-scale synthesis of chiral drugs. To realize that, we focus on 1) the design and the synthesis of novel chiral catalysts, 2) the development of practical reagents, and 3) the development of novel methodology for C-C, C-O, C-N, or C-B bond formations.
Related Keyword
- "Cu-Catalyzed Synthesis of 2-Silyl-1,3-butadienes from Allenols and Applications to One-Pot Synthesis of Tetrasubstituted Arylsilanes", Organic Letters, v.25, no.49, pp.8932 - 8936
- "Nickel-Catalyzed Mono- and Dihydrosilylation of Aliphatic Alkynes in Aqueous and Aerobic Conditions", ACS Catalysis, v.14, no.7, pp.5077 - 5087
- "Synthesis of alpha-Borylmethyl-(E)-allylborons via Cu-Catalyzed Diboration of 1-Substituted Allenols and Their Application in Stereoselective Aldehyde Allylation", ACS Catalysis, v.13, no.17, pp.2351 - 2358
- "Synthesis of (Z)-Allylsilanes by Cu-Catalyzed Regioselective Protosilylation of Allenes via a Single-Electron Process", ACS Catalysis, v.15, no.3, pp.2380 - 2388
연구분야
미래유망 신기술(6T)
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70.
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700.
70000. 기타(6T외)
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국가과학기술표준분류
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NC. 화학
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NC02. 유기화학
NC0202. 유기합성/전합성
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NC. 화학
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NC03. 무기화학
NC0303. 유기금속화학
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NC. 화학
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NC02. 유기화학
NC0203. 유기합성방법론
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NC. 화학
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NC02. 유기화학
NC0208. 의약/조합 화학
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