• Bulletin of the Korean Chemical Society
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• 제6권6호
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• pp.358-361
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• 1985

Thianthrene cation radical perchlorate (1) reacted with azo-bis-2-phenoxy-2-propane (6) to give thianthrene (2), cisthianthrene-5,10-dioxide, 5-(p-hydroxyphenyl) thianthrenium perchlorate (10), acetone, phenol, and 5-(2-propenyl) thianthrenium perchlorate (11) when the mole trtio of 1 to 6 was 1:1. Among the products, 11 was a new compound. However, when the corresponding mole ratio was 5:1, 11 was not formed. Similar result was obtained for azo-bis-2-(p-nitrophenoxy)-2-propane.

• Bulletin of the Korean Chemical Society
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• 제20권8호
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• pp.935-938
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• 1999

Reactivity and reaction mechanism for the reactions of 1,1'-(azodicarbonyl) dipiperidine with triphenylphosphines are investigated using kinetic method. The cation radical, Ph3P and the anion radical, -N-N - are produced during the course of the reaction. The cation radical is formed by the transfer of an electron from phosphorus to the nitrogen atom. The anion radical is formed by the addition of the one electron to the azo rad-ical. The rate constants are decreased by electron withdrawing groups while they are increased by electron donating groups present in triphenylphosphine. The electron density increases on nitrogen, while positive charge is developed on phosphorus in the transition state.

• Journal of Photoscience
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• 제10권1호
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• pp.61-69
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• 2003

Mechanistic as well as synthetic aspects of the photoinduced electron transfer reactions of epoxy ketones, bromomethyl-substituted benzocyclic ketones, and tribromomethyl-substituted cyclohexadienones with amines are described.

• 생명과학회지
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• 제17권8호통권88호
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• pp.1100-1103
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• 2007

합성항산화제 3종과 17종의 식물 추출물을 이용하여 양성자 빔을 1,000, 5,000, 10,000 Gray 수준으로 처리하여 에너지양에 따른 항산화 활성에 미치는 영향을 탐색 하고자 DPPH radical 소거능 과 ABTS cation radical 소거능의 활성에 대하여 조사하였다. 이중 6종류의 시료는 양성자 빔을 조사한 결과 활성이 감소하였으며, 2종류의 시료는 활성변화가 없었으며, 12종류의 시료는 활성이 증가하였다. DPPH radical 소거 효과는 1,000 Gray 에서 마황은 60%, 괄루인은 5,000 Gray 에서 77.8%로 활성이 증가하는 경향을 나타내었다. ABTS cation radical 소거효과에서 토천궁은 1,000 Gray의 양성자 빔을 조사한 결과 38.5% 활성이 감소하였으며, 합성 항산화제는 활성변화가 거의 없으나, 뼝쑥 추출물은 5,000 Gray에서 $IC_{50}$값이 2.4 ${\mu}g/ml$로 BHT의 $IC_{50}$값 2.3 ${\mu}g/ml$과 유사하였다.

• 한국약용작물학회지
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• 제17권1호
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• pp.15-20
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• 2009

This study was carried out in order to determine the biological activities such as antioxidant activities in nine cultivars of Momordica charantia L. (Korea, China, Japan and Philippine native cultivars). Their antioxidant activities were measured using DPPH free radical scavenging, ABTS cation radical scavenging, and Nitrite scavenging ability. The highest total polyphenol content (16.82 ${\mu}g/m{\ell}$) measured in the native Korea cultivar, and this value was 4.0 ${\mu}g/m{\ell}$ higher than that of the 'Verde Beuhas' cultivar (12.82 ${\mu}g/m{\ell}$). The 'Peacock' cultivar had the highest total flavonoid amount which was 4.38 ${\mu}g/m{\ell}$. The free radical scavenging activity using DPPH method was the highest in the native China cultivar ($RC_{50}$ = 102.6 ${\mu}g/m{\ell}$). ABTS cation radical scavenging activity according to cultivars was significantly higher in 'Peacock'. Nitrite scavenging ability showed the most remarkable effect at the pH 1.2, exhibited to 81.5${\sim}$86.9% by addition of ethanol extract 1${\mu}g/m{\ell}$ from Momordica charantia L. These results suggest that Momordica charantia L. had the potent biological activities, and that their activities exhibited differently depending on cultivars.

• Bulletin of the Korean Chemical Society
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• 제9권3호
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• pp.144-149
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• 1988

Reaction of thianthrene cation radical perchlorate (1) with 1-methyl-4-benzenesulfonylaminobenzene (10) afforded thianthrene (5), N-(4-tolyl)-N-thianthrenylbenzenesulfonamide (14), 1-methyl-3-[N-(4-tolyl)-N-benzenesulfonyl-amino- 4-benzene-sulfonylaminobenzene (16), cis-thianthrene-5,10-dioxide (17), 5-(3'-methyl-6-benzenesulfonylaminobenzene)thian threnium perchlorate (18), and benzenesulfonate. In the meantime, reaction of 1 with 1-ethyl-4-benzenesulfonylaminobenzene (12) afforded 5, 1-ethyl-3-[N-(4-ethylphenyl)-N-benzenesulfonyl]a mino-4-benzenesulfonylaminobenzene (19), 1-benzenesulfonyl-amino-4-[1-(2-benzenesulfonyla mino-5-ethylphenyl)ethyl]benzene (20), and 1-(1-acetamidoethyl)-4-benzenesulfonylaminobenz ene (21). The formations of these products except for 18 and benzenesulfonate could be rationalized by assuming a sulfonamidyl radical as an intermediate.

• Bulletin of the Korean Chemical Society
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• 제10권6호
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• pp.509-514
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• 1989

Reactions of thianthrene cation radical perchlorate (1) with N-(p-methoxyphenyl)benzenesulphonamide (14) in acetonitrile at room temperature afforded various products : thianthrene (3), N-(p-hydroxyphenyl)benzenesulphonamide (16), benzenesulphonamide (18), hydroquinone (20); 5-(5-benzenesulphonamido-2-methoxyphenyl)-thia nthrenium perchlorate(21), 2-benzenesulphonamido-2'-hydroxy-5,5'-dimethoxy biphenyl(24), 2-benzenesulphonamido-2',5'-dihydroxy-5-methoxy -biphenyl(25), and a traceable amount of p-quinone(23). The formations of part of (3) and (21) can be explained by either disproportionation or half-regeneration mechanism but those of the remainders by diverse reactions of sulphonamidyl radical (27) derived from (14) (through single electron transfer, followed by deprotonation processes). Similar results were observed from the reaction with N-(p-methoxyphenyl)methanesulphonamide (15).

• Bulletin of the Korean Chemical Society
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• 제13권6호
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• pp.694-695
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• 1992

• Bulletin of the Korean Chemical Society
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• 제17권9호
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• pp.775-777
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• 1996

• Bulletin of the Korean Chemical Society
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• 제16권12호
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• pp.1225-1227
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• 1995