• Bulletin of the Korean Chemical Society
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• v.6 no.6
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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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• v.20 no.8
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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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• v.10 no.1
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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.

• Journal of Life Science
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• v.17 no.8 s.88
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• pp.1100-1103
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• 2007

In proton therapy, the Bragg peak is spread out by modulating or degrading the energy of the particles to cover a well-defined target volume at a given depth. Proton transfer plays a key role in a variety of biological, the origin of the elements, tests of the standard model along with applications in medicine, industry and chemical phenomena such as water autoionization, fast proton diffusion, acid-base neutralization. We have studied the radiolysis of various natural resources and have evaluated the antioxidant activity of radiolysis products by proton beam. The most of antioxidant activities of natural resources were decreased with increasing proton fluence. Proton beam induced antioxidant activities both in 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) assay and 2,2'-azinobis(3-ethylbenzot hialozinesulfonic acid) cation radical $(ABTS^{.+})$ assay by a dose dependent fashion.

• Korean Journal of Medicinal Crop Science
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• v.17 no.1
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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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• v.9 no.3
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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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• v.10 no.6
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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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• v.13 no.6
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• pp.694-695
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• 1992

• Bulletin of the Korean Chemical Society
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• v.17 no.9
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• pp.775-777
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• 1996

• Bulletin of the Korean Chemical Society
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• v.16 no.12
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• pp.1225-1227
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• 1995