• 대한화학회지
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• 제58권4호
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• pp.381-387
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• 2014

A series of new $N^7$-tetrazolo[5,1-f ]-1,2,4-triazin-8-(7H)-one derivatives 4-16 were designed and synthesized from 3 with different reagents. The newly prepared compounds were characterized by spectral data and screened for their antimicrobial activities against various bacteria and fungi strains.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.362.4-363
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• 2002

Costunolide which is known as a chemopreventive drug is a sesquiterpene compound isolated from Magnolia Sieboldii. and has antitumor and antiinflamatory activities. it is very hard to collect enough amount of natural extracts of costunolide for the activity studies. therfore. synthesis of costunolide derivatives is honestly needed. the aim of this research is to develope new methods for costunolide synthesis and to test biological activities. (omitted)

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.341.3-342
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• 2002

The interest in polyhydroxyamines is based in their biological activity as enzyme inhibitors. and as starting materials in the synthesis of more complex compounds. Polyhydroxyamines is that amine group is continuing structurally with hydroxy groups and has become important target of the synthesis strategy because of the chirality control of amine group and each hydroxy groups. (omitted)

• Bulletin of the Korean Chemical Society
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• 제30권1호
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• pp.43-48
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• 2009

The synthesis of coumarin-based natural products and their derivatives is described. In vitro MDR reversal activities of the synthesized compounds were evaluated in P-glycoprotein over-expressing human sarcoma cell line MES-SA/DX5. Some of the coumarin derivatives were found to show potent MDR reversal activity. In particular, pyridyl derivative (15e) exhibited more potency than verapamil.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.238.2-238.2
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• 2003

The synthesis of a new series of 1${\beta}$-methylcarbapenems having the substituted aminoethyl-carbamoylpyrrolidine moiety is described. Their in vitro antibacterial activities against both Gram-positive and Gram-negative bacteria were tested and the effect of substituent on the pyrrolidine ring was investigated. In particular. the compound 11 g having piperazinyl urea moiety showed the most potent antibacterial activity.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.175.1-175.1
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• 2003

Galactosyl ceramides paly important roles in biological system as immunomodulator and essential constituents of membranes and cell walls. An efficient synthesis of $\alpha$-galactosyl ceramide, KRN 7000, derived from marine sponge Agelas mauritianus as accomplished via a short reaction involving the coupling ceramide moiety and trichloroacetimidate as glycosylation donor. We could synthesize $\alpha$-galactosyl ceramide stereoselectivity without $\beta$-anomer formation on a multigram scale.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.188.1-188.1
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• 2003

The antiparasitic agent apicidin, which was recently isolated from cultures of Fusarium Pallidoroseum, belongs to a rare group of cyclictetrapeptide fungal metabolites. Apicidin inhibits protozoal HDAC and is orally active against Plasmodium berghei malaria in mice. The biological activity of apicidin appears to be attributable to inhibition of apicomplexan HDAC at low nanomolar concentrations. In the present, we have worked about the synthesis of new apicidin derivatives and discovered that apicidin and some derivatives have mild antitumor activity. (omiited)

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.342.2-342.2
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• 2002

The ${\beta}$-turn has been implicated as an important conformation for biological recognition of peptides or proteins. Benzodiazepine classes have been known as one of the non peptide ${\beta}$-turn mimic scaffolds. We have developed an efficient approach for the synthesis and derivatization of a scaffold of hydroxytetrahydrodizepinone class in order to screen compound library in various protein targets for new lead generations as well as for structure activity relationships of the scaffold. (omitted)

• 한국가스학회지
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• 제18권4호
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• pp.63-67
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• 2014

Fischer-Tropsch 합성은 주로 긴 carbon 사슬을 가지고 있는 높은 점도의 왁스를 product로 생산한다. 촉매 고정층 반응기를 이용하여 Fischer-Tropsch 합성을 수행할 경우, 왁스는 촉매입자의 표면에서 생산되어 촉매입자 표면에 흡착되어 있다. 이런 왁스의 hold-up 현상이 반응기 전체의 압력강하는 증가시키고 내부 흐름을 막는 문제를 일으킨다. 따라서 반응기 내부에 왁스가 hold-up되는 현상에 대한 모델링을 통해 왁스 hold-up 현상을 최소화 할 수 있는 반응기 및 촉매 입자의 크기를 결정하는 설계 과정이 필요하다. 본 연구에서는 왁스가 hold-up된 촉매 입자와 기체 흐름 사이의 대류 물질 전달 실험 모델을 이용하여 반응기 구조 및 운전 조건을 고려할 수 있는 반응기 내부 왁스 hold-up 모델을 개발하였다. 개발된 모델은 실험 데이터를 제공한 Knochen의 연구 결과와 비교하여 모델의 우수성을 검증하였다. 이 모델을 이용하여 반응기의 길이와 단면이 반응기 내부 왁스 hold-up 현상에 어떻게 영향을 미칠 수 있는지 분석해 보았다.

• Bulletin of the Korean Chemical Society
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• 제28권9호
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• pp.1562-1566
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• 2007

1-Alkenyl-2,3-dimethylimidazolium tetrafluoroborate ionic liquids having an olefinic substituent were synthesized and characterized. Among them, [AMMIm]BF4 with an allyl group showed lower viscosity, higher ionic conductivity, and a wider electrochemical window compared with its analogue having a saturated alkyl substituent. An EDLC with [AMMIm]BF4 showed better performance than that with [PMMIm]BF4, too.