• Bulletin of the Korean Chemical Society
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• 제25권12호
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• pp.1850-1854
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• 2004

Recently a fullerene isoxazoline was reported as an example for nanoscale connectors in molecular electronic devices. The construction of nanoscale devices is a potentially important area of technology. By using the semiempirical PM3 calculation, we optimized the structures for two fullerene isoxazoline derivatives and thirteen regioisomers of the second addition of a nitride oxide to a fullerene isoxazoline derivative. Our results suggest that fullerene isoxazoline derivatives could be used as nanoscale connectors with the possibility of attaching of spacer units in a specific angle arrangement.

• 농약과학회지
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• 제12권2호
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• pp.197-200
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• 2008

Thiophene에 다양한 치환기를 가진 5-benzyloxymethyl-1,2-isoxazoline 유도체들을 합성하였으며 이들의 제초활성을 온실의 논조건에서 시험하였다. 대부분의 화합물은 좋은 제초활성을 보였다. 특히 화합물 3d, 3e, 3f는 피, 물달개비 등에 대하여 0.063 kg/ha 정도의 약량에서도 강한 제초활성을 보이면서도 이앙벼에는 약해가 거의 나타나지 않는 선택성을 갖고 있었다.

• 농약과학회지
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• 제11권2호
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• pp.67-71
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• 2007

Thiophene을 포함한 isoxazoline 구조를 가진 화합물 중에서 제초활성이 매우 좋을 것으로 예상된 5-benzyloxymethyl-3-(thiophen-5-yl)-1,2-isoxazoline 유도체들을 합성하였고 이들의 제초활성을 논조건에서 시험하였다. 대부분의 화합물의 제초활성은 매우 강하였으며 이앙벼에는 약해가 거의 나타나지 않았다. 각종 잡초에 대한 제초활성이 우수할 뿐 아니라, 낮은 농도에서 높은 제초활성을 보여 신규제초제 후보물질로서의 가능성을 보였다.

• Bulletin of the Korean Chemical Society
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• 제31권5호
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• pp.1305-1308
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• 2010

Regioselective perfluorinated isoxazolidine (5 and 7), isoxazoline (9) and 1,2-addition products (6 and 8) having a long alkyl chain functionality have been prepared by 1,3-dipolar cycloaddition between a 1,3-dipole (NH-nitrone or nitrile oxide) and dipolarophile (perfluoro-2-methyl-2-pentene or styrene), respectively. Interestingly, unusual extended conjugated form of isoxazoline adduct (10) was obtained by dehydrofluorinated reaction from the corresponding perfluorinated isoxazoline adduct (9) which was derived from cycloadition between the perfluorinated long alkyl nitrile oxide 1,3-diplole and styrene olefin. This synthetic methodology of heterocyclic compound having a long alkyl chain functionality is useful for the designing of synthetic strategy and potential self-assembled monolayers (SAM) application. These derivatives were characterized by IR, $^1H$ and $^{19}F$ NMR, and MASS analysis.

• 대한화학회지
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• 제33권6호
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• pp.673-676
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• 1989

• Biomolecules & Therapeutics
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• 제2권2호
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• pp.155-160
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• 1994

Human immunodeficiency virus type 1 (HIV-1) protease is essential for the replication of the virus and it is therefore an attractive target for antiviral drugs of HIV-1. Several dipeptide isosteres containing 2-isoxazoline or $\alpha$-hydroxy ketomethylene have been synthesized and their inhibitory effects on the HIV-1 protease examined. The enzymatically active HIV-1 protease was purified to homogeniety from E. coli transformed with a recombinant plasmid (pMAL-pro) containing the entire gene encoding the protease. The purified protease had the substrate specificity with Km value of 9.8$\mu$M when an undecapeptide His-Lys-Ala-Arg-Val-Leu-(p-nitro)Phe-Glu-Ala-Nle-Ser-amide was used as a substrate, and the products from the substrate after specific cleavage by HIV-1 protease were analyzed by HPLC. The synthetic compounds containing dipeptide isosteres showed specific inhibitory effects while a dipeptide isostere containing an isoxazoline ring inhibited the HIV-1 protease competitively with Ki value of 500 $\mu$M. Even if the inhibition effects of HIV-1 protease were not very high, these novel dipeptide isosteres can be used as key structural moieties for developing specific inhibitors of HIV-1 protease.

• Bulletin of the Korean Chemical Society
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• 제30권8호
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• pp.1873-1876
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• 2009

• Bulletin of the Korean Chemical Society
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• 제17권1호
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• pp.2-4
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• 1996

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1993년도 제2회 신약개발 연구발표회 초록집
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• pp.121-121
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• 1993

Angiotensin Converting Enzyme (ACE)의 효과적인 억제제를 합성하기 위하여 ketomethylene dipeptide isoster와 2-isoxazoline dipeptide isoster를 얻는 방법을 확립하였다. 상기 등입체성 분자들은 아미노산으로부터 유도된 아미노 니트릴 옥사이드의 고리더함반응을 이용하여 효율적으로 합성하였다. 얻어진 이 화합물로부터 ACE 억제제 후보물질 (1, 2)의 합성이 연구되고 있다.

• 농약과학회지
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• 제3권3호
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• pp.68-70
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• 1999

Hexahydro-1,2-bertzisoxazol-4-ols prepared from the diastereoselective reductions of 3-aryl-3a,4,5,6,7,7a-hexahydro-1,2-benzisoxazol-4-ones were reacted with benzyl chloride in the presence of sodium hydride to give new 4-benzyloxy-3a,4,5,6,7,7a-hexahydro-1,2-benzisoxazoles, which showed good herbicidal activity together with excellent selectivity on rice under submerged paddy conditions.