• Bulletin of the Korean Chemical Society
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• 제33권2호
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• pp.739-741
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• 2012

• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3193-3194
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• 2013

• Bulletin of the Korean Chemical Society
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• 제17권8호
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• pp.678-679
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• 1996

• 대한화학회지
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• 제55권4호
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• pp.666-672
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• 2011

Vanadium 치환체인 polyoxometalate 1, [Cu(2,2'-bipy)]$[Cu(2,2'-bipy)_2]_2[PMo_8V_6O_{42}]{\cdot}1.5H_2O$을 가지고 있는 inorganicorganic complex의 촉매 활성도를 Biginelli 반응에 적용하여 연구하였다. Dihydropyrimidinones를 one-pot 합성하는 반응에서, $H_3PMo_{12}O_{40}$ 촉매 보다[Cu(2,2'-bipy)]$[Cu(2,2'-bipy)_2]_2[PMo_8V_6O_{42}]{\cdot}1.5H_2O$ 촉매가 더 좋은 결과를 나타내었다.

• 대한화학회지
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• 제63권6호
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• pp.435-439
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• 2019

An efficient one pot multicomponent synthesis of pyrimidinone derivatives of Biginelli type is described. 4-amino-6-aryl-pyrimidine-5-carbonitrile molecules were synthesized efficiently via three-component Biginelli-type condensation of aldehyde, malononitrile, and semicarbazone as urea substituent in the presence of a catalytic amount of PEG-400 as green medium under microwave irradiation. The reactions proceeded efficiently in the presence of microwave radiation to afford the desired products in good to excellent yields. Products have been confirmed by IR, and NMR spectral analysis. All the molecules were tested for their antimicrobial activity against E. coli, S. aureus, P. aeruginosa and C. tropicalis. Some of the compounds have shown moderate to good inhibition efficiency against both gram-positive and gram-negative bacteria. The potent activity was observed against the fungal species with minimum inhibition concentration 12.5 ㎍/mL.

• 공업화학
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• 제28권5호
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• pp.495-500
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• 2017

본 연구에서는 마그네슘 이온 및 (3-aminopropyl)triethoxysilane (APTES)으로 표면에 amine group이 부착된 아미노클레이를 합성(AC)함과 동시에 천연 화합물인 프로폴리스 및 황련 추출물을 클레이 시트 사이에 삽입한 클레이를 합성(PIAC, CIAC)하였다. 주사전자현미경, 입도 분석법, FT-IR, TGA 및 XRD를 통해 클레이의 합성 및 천연 화합물의 삽입을 확인하였고, 특히 XRD data에서 천연 화합물의 삽입에 따른 층간거리(d-space)를 분석함으로써 명확하게 그 특성을 결정하였다. 또한 천연 화합물이 삽입된 클레이인 PIAC 및 CIAC의 경우 삽입되지 않은 아미노클레이(AC)에 비해 항균성이 향상된 것을 최소저해농도(MIC) 분석을 통해 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제30권3호
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• pp.551-555
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• 2009

The ytterbium catalyst immobilized on the cross-linked poly(4-vinylpyridine/styrene) copolymer (P/S-Yb) was applied in the Mannich-type, three component one-pot synthesis of $\beta$-aminoketones. This catalytic system showed excellent catalytic activity and selectivity which resulted in the exclusive formation of $\beta$-aminoketone. The applicability of this immobilized catalyst system was shown by the reusability test and again highlighted by the synthesis of a $\beta$-aminoketone library using a broad range of substrates.

• 대한화학회지
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• 제53권1호
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• pp.90-94
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• 2009

• Bulletin of the Korean Chemical Society
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• 제33권8호
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• pp.2679-2682
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• 2012

A simple one-pot synthesis of two derivatives of 1,4-dihydropyridines has been described under reflux conditions using copper iodide nanoparticles (CuI NPs) as a catalyst in high yields. This method demonstrated four-component coupling reactions of aldehydes and ammonium acetate via two pathways. In one route, the reaction was performed using 2 eq ethyl acetoacetate while in the other one 1 eq ethyl acetoacetate and 1 eq malononitrile were used. The CuI NPs was reused and recycled without any loss of activity and product yield. It is noteworthy to state that wide range of the 1,4-dihydropyridines have attracted large interest due to pharmacological and biological activities.

• Bulletin of the Korean Chemical Society
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• 제31권4호
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• pp.863-868
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• 2010

Yttrium(III) acetate hydrate-catalyzed novel synthesis of 3,4-dihydropyrimidin-2(1H)-(thio)one derivatives was achieved through one-pot three-component condensation of diversified aldehydes, $\beta$-ketoesters and urea or N-methylurea or thiourea with a molar ratio of 1:1:1.4. In comparison to the classical Biginelli approach, this catalytic method has the advantages of short reaction time and improved product yield.