이선우 교수
Sun-woo Lee
서울대학교 불어불문학과 · 화학
연구실 소개
이선우 교수의 연구실은 주로 팔라듐 촉매를 활용한 고도로 선택적인 유기합성 반응을 중심으로 연구를 전개하고 있습니다. 특히 산화이ند올 유도체의 합성, 에스터 및 보호된 아미노산의 알릴화 반응, 알킨(carboxylic acid)을 이용한 탈카복실화 연합 반응 등에서 높은 수율과 반응 조건의 온화함을 실현합니다. 또한, 유기촉매 반응의 메커니즘 해석과 새로운 촉매 체계 개발을 통해 합성 화학의 효율성과 응용 가능성을 확장하고 있습니다.
연구 현황
연구 성과 추이
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주요 논문
15Catalysts comprised Pd(OAc)(2) and either PCy(3) or sterically hindered N-heterocyclic carbene ligands provide fast rates for a palladium-catalyzed synthesis of oxindoles by amide alpha-arylation. This catalyst system allowed for room-temperature reactions in some cases and reactions of aryl chlorides at 70 degrees C. Most important, reactions occurred in high yields under mild conditions to form the quaternary carbon in alpha,alpha-disubstituted oxindoles. The combined inter- and intramolecular
ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTPalladium-Catalyzed α-Arylation of Esters and Protected Amino AcidsSunwoo Lee, Neil A. Beare, and John F. HartwigView Author Information Department of Chemistry Yale University, P.O. Box 208107 New Haven, Connecticut 06520-8107 Cite this: J. Am. Chem. Soc. 2001, 123, 34, 8410–8411Publication Date (Web):August 3, 2001Publication History Received17 April 2001Revised1 July 2001Published online3 August 2001Published inissue 1 August 2001https://pubs.
[reaction: see text]. A simple, palladium-catalyzed method to convert aryl halides to the parent anilines using lithium bis(trimethylsilyl)amide (LiN(SiMe3)2) is reported. The reaction is catalyzed by Pd(dba)2 and P(t-Bu)3 and can be run with as little as 0.2 mol % of catalyst. The reaction is faster than competing generation of benzyne intermediates and, therefore, provides the aniline products regiospecifically.
Pseudomonads from environmental sources vary widely in their sensitivity to cadmium, but the basis for this resistance is largely uncharacterized. A chromosomal fragment encoding cadmium resistance was cloned from Pseudomonas putida 06909, a rhizosphere bacterium, and sequence analysis revealed two divergently transcribed genes, cadA and cadR. CadA was similar to cadmium-transporting ATPases known mostly from gram-positive bacteria, and to ZntA, a lead-, zinc-, and cadmium-transporting ATPase fr
The decarboxylative coupling of alkynyl carboxylic acids is an attractive area of research in organic chemistry, because the structure of aryl alkyne is one of the important building blocks for the synthesis of p-conjugated compounds. The use of alkynyl carboxylic acid as an alkyne source has several advantages in handling and storage. As a catalyst, palladium, copper, nickel, and silver were employed in the decarboxylative coupling reactions. The formation of C–C (sp2–sp, sp–sp and sp3–sp), C–N
Arylsulfonyl compounds are among the most important compounds in pharmaceutical and medicinal chemistry. Hence, a wide variety of sulfonylation methods have been reported recently. This review summarizes arylsulfonylation methodologies developed in the last 5 years and includes two major categories. The first entails direct arylsulfonylation and the second multicomponent arylsulfonylation. In direct arylsulfonylation, arylsulfonyl reagents react with C–H activated compounds, alkynes, and alkenes
We have fabricated boron carbide thin films on Si(111) and other substrates by plasma-enhanced chemical-vapor deposition (PECVD). The PECVD of boron carbides from nido-cage boranes, specially nido-pentaborane(9) (B5H9), and methane (CH4) is demonstrated. The band gap is closely correlated with the boron to carbon ratio and can range from 0.77 to 1.80 eV and is consistent with the thermal activation barrier of 1.25 eV for conductivity. We have made boron carbide by PECVD from pentaborane and meth
This study examined the relationship between material adversities due to pandemic crisis, institutional trust, and subjective well-being and mental health among middle-aged and older adults aged 50+ in Europe. The study used a cross-sectional design to examine Eurofound COVID-19 survey data collected from 27 European countries in April 2020. A total of 31,757 European middle aged and older adults aged 50 + were analyzed (Mean = 59.99, <i>SD</i> = 7.03). Analysis focused on the financial impact a
In this paper, a robust adaptive tracking control scheme is proposed for compensation of the stick-slip friction in a mechanical servo system. The control scheme has a sliding control input to compensate friction forces. The gain of the sliding control input is adjusted adaptively to estimate the linear bound of the stick-slip friction. By introducing the sliding control input, the global stability and the tracking error asymptotic convergence to the predetermined boundary are established via Ly
Graphene mechanical resonators are the ultimate two-dimensional nanoelectromechanical systems (NEMS) with applications in sensing and signal processing. While initial devices have shown promising results, an ideal graphene NEMS resonator should be strain engineered, clamped at the edge without trapping gas underneath, and electrically integratable. In this Letter, we demonstrate fabrication and direct electrical measurement of circular SU-8 polymer-clamped chemical vapor deposition graphene drum
Abstract Copper‐catalyzed coupling reaction of 2‐iodobenzoic acids and alkynes such as terminal acetylenes, alkynyl carboxylic acids, and trimethylsilylacetylene selectively afforded isocoumarins and phthalides in the presence of cesium carbonate (Cs 2 CO 3 ) and dimethyl sulfoxide (DMSO). Among the regioselective products, only the 6 ‐endo‐dig product, isocoumarin, was formed at 100 °C, and the 5‐ exo‐dig product, phthalide, was formed as a major product at 25 °C. A variety of alkynes produced
Abstract A variety of aryl bromides were coupled with propiolic acid in the presence of 1,8‐diazabicyclo[5.4.0]undec‐7‐ene (DBU) and catalyst Pd(PPh 3 ) 4 to afford the corresponding arylalkynecarboxylic acids in good yields at low temperature. This method showed good tolerance toward functional groups such as alkoxy, ketone, ester, aldehyde, cyano, nitro, and hydroxy. Under these conditions, propiolic acid showed higher reactivity than any other compound containing terminal alkyne groups. Accor
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