• Bulletin of the Korean Chemical Society
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• 제32권2호
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• pp.472-476
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• 2011

Sodium chlorate/hydrochloric acid mixtures were used to chlorinate activated arenes and the $\alpha$-position of ketones. This chlorination method was used to produce selectively mono-, di-, and trichlorinated compounds by controlling the molarity of sodium chlorate. This reagent proved to be much more efficient and easier to handle than chlorine gas.

• Bulletin of the Korean Chemical Society
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• 제33권11호
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• pp.3559-3564
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• 2012

An efficient one-pot synthesis of ${\beta}$-acetamido ketones was accomplished by AgOTf-catalyzed multicomponent reactions of substituted acetophenones with aromatic aldehydes and acid chloride in acetonitrile in high yields. The methods offer several significant advantages of easy handling, mild reaction conditions, and use of effective and non-toxic catalyst.

• 한국식품영양과학회지
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• 제24권3호
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• pp.420-426
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• 1995

Volatile compounds in raw oyster and oyster hydrolysate produced with protease were compared by vacuum simultaneous steam distillation-solvent extraction/gas chromatography/mass spectrometry. Sixty-two volatile compounds were detected in both samples. Of these, 57 were positively identified, composed mainly of aldehydes(12), ketones(9), alcohols(14), nitrogen-containing compounds(9), acids(6), terpenes(4), and miscellneous compounds(8). Levels of acids decreased after hydrolysis, whereas several other compounds such as aldehydes, ketones, and nitrogen containing compounds increased. Pyrazines, found in high abundance, were only detected in oyster hydrolysate.

• Bulletin of the Korean Chemical Society
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• 제32권10호
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• pp.3760-3762
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• 2011

• Bulletin of the Korean Chemical Society
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• 제4권5호
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• pp.197-200
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• 1983

The Diels-Alder cycloaddition reactions between dienes and allenic ketones were studied theoretically using CNDO/2 method. It was found that the reaction is a neutral electron demand type with matrix element control and the reactivity, the regio- and stereo-selectivities can be correctly predicted based on interaction energies calculated with the 4-center FMO formalism.

• Bulletin of the Korean Chemical Society
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• 제16권4호
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• pp.349-355
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• 1995

Bromo-and chlorotrimethylsilane react with selenium dioxide in halocarbon solvents and generate selenium oxybromide and oxychloride, respectively. These in-situ generated oxyhalides turned out to be very efficient for selective bromination and chlorination of aldehydes and ketones. Under carefully controlled reaction conditions, second and third introduction of halogens into carbonyl compounds can be greatly suppressed, and high yields of monohalo compounds were obtained. The product ratios of this halogenation reactions can be best explained if the reactions are assumed to involve intermediate β-ketoselenenyl chlorides.

• 한국식품조리과학회지
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• 제17권1호
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• pp.55-59
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• 2001

신선 및 동결 건조된 두메부추 잎을 연속수증기 증류추출 장치로 증류하여 얻어진 정유성분을 GC 및 GC-MS로 분석하여 신선한 시료에서 11종의 hydrocarbons 0.136ppm 9종의 aldehydes 0.278ppm, 4종의 alcohols 0.025ppm, 2종의 esters 2.328ppm, 7종의 acids 0.545ppm, 4종의 ketones 0.037ppm 및 9종의 sulfur containing compounds 0.117ppm의 총 46종의 성분을 확인하였다. 동결 건조한 두메부추 잎에서는 8종의 hydrocarbons 1.357ppm 5종의 aldehydes 0.498ppm, 3종의 alcohols 0.094ppm, 5종의 esters 0.720ppm, 2종의 acids 0.069ppm 3종의 ketones 0.163ppm 및 4종의 sulfur containing compounds 0.039ppm을 포함하여 총 30종의 향기성분이 확인되었다. 전자코의 분석 결과, 제1주성분 값의 기여율이 0.987을 나타내어 제1주성분이 두메부추와 부추를 총괄하는 정보로 사용될 수 있음을 알 수 있다. 신선한 두메부추는 제1주성분 값이 0.5부근에 집중된 분포를 보이고, 신선한 부추는 -0.5부근에 분포되어 있어 신선한 두메부추와 신선한 부추의 휘발성 향기성분 패턴이 다름을 알 수 있었다. 또한 동결 건조된 시료의 경우, 두메부추는 제1주성분 값 0을 중심으로 -쪽에 분포되어 있고, 부추는 +부근에 분포되어 있어 동결 건조된 시료의 휘발성 향기성분 패턴도 차이가 있었다.

• 대한화학회지
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• 제33권5호
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• pp.522-529
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• 1989

팔라듐 촉매를 이용하여 할로겐화 비닐의 CO 첨가반응과 짝지음 반응을 동시에 진행시키는 CO 첨가 호모 짝지음 반응을 실시하여 비교적 좋은 수득률로 대칭 디비닐케톤 및 디비닐 ${\alpha}$-디케톤을 합성하였다. 촉매로는 palladium(II) acetate에 2mol%의 리간드를 사용하고 염기는 3당량의 tributylamine, 극성 용매를 사용하여 10기압의 일산화탄소 존재 하에 $100^{\circ}C$에서 반응을 실시한 경우 디비닐 ${\alpha}$-디케톤을 가장 좋은 수득률로 얻을 수 있었으며, 일산화탄소 상압 하에서는 주로 디비닐케톤이 합성되었다. 또한, 여러가지 할로겐화 비닐에 대해 위와 같은 반응조건으로 반응을 실시해 본 결과 예상한 대로 순조롭게 반응이 진행되어 여러가지의 디비닐케톤 및 디비닐 ${\alpha}$-디케톤을 선택적으로 합성할 수 있음을 확인하였다.

• 대한화학회지
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• 제55권5호
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• pp.751-755
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• 2011

A doubly tethered chiral stationary phase (CSP) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid was applied to the resolution of various aryl ${\alpha}$-aminoalkyl ketones with the use of 80% ethanol in water containing 10 mM sulfuric acid as a mobile phase. The chiral resolution was quite successful, the separation factors (${\alpha}$) and the resolutions ($R_S$) being in the range of 1.39-2.05 and 3.18-5.22, respectively. The separation factors (${\alpha}$) on the doubly tethered CSP were slightly worse than those on the corresponding singly tethered CSP. However, the resolutions ($R_S$) on the doubly tethered CSP were generally greater than those on the corresponding singly tethered CSP. The chromatographic behaviors for the resolution of aryl ${\alpha}$-aminoalkyl ketones on the doubly tethered CSP were demonstrated to be dependent on the type and the content of the organic and acidic modifiers in aqueous mobile phase and the column temperature.

• Bulletin of the Korean Chemical Society
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• 제35권12호
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• pp.3571-3575
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• 2014

Proteasome, a multicatalytic protease complex, has been validated as a promising therapeutic target in oncology. Carfilzomib (Kyprolis$^{(R)}$), a tetrapeptide epoxyketone, irreversibly inhibits the chymotrypsin-like (CT-L) activity of the proteasome and has been recently approved for multiple myeloma treatment by FDA. A chemistry effort was initiated to discover the compounds that are reversibly inhibit the proteasome by replacing the epoxyketone moiety of carfilzomib with a variety of ketones as reversible and covalent warheads at the C-terminus. The newly synthesized compounds exhibited significant inhibitory activity against CT-L activity of the human 20S proteasome. When the compounds were tested for cancer cell viability, 14-8 was found to be most potent in inhibiting Molt-4 acute lymphoblastic leukemia cell line with a $GI_{50}$ of $4.4{\mu}M$. Cytotoxic effects of 14-8 were further evaluated by cell cycle analysis and Western blotting, demonstrating activation of apoptotic pathways.