http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
1-Chloro-1-phenyl-2-carboethoxy-2-cyanoethene 유도체에 대한 thioglycolic acid 치환제의 합성
이영행,이채호,이갑상,이만구 圓光大學校 1984 論文集 Vol.18 No.2
The substitution products of thioglycolic acid to the derivatives of 1-chloro-1-phenyl-2-carboethoxy-e-cyano ethene synthesized 1-Chloro-1-phenyl-2-carboethoxy-2-cyanoethene [Ⅴ], 1-chloro-10(4-chlorophenyl)-2-carboethoxy-2-cyanoethene[Ⅳ] and 1-chloro-1-(4-methoxyphenyl)-2-carboethoxy-2-cyanoethene[Ⅶ] undergo substitution reactions with thioglycolic acid to form s-[(1-phenyl-2-carboethoxy-2-cyano) ethenyl]-thioglycolic acid s-[(1-(4-chlorophenyl)-2-carboethoxy-e-cyano] ethenyl]-thioglycolic acid and s-[1-(4-methoxyphenyl)-2-carboethoxy-2-cyano] ethenyl]-thioglycolic acid, respectively. The structure of products were identified by elemental analysis, potentiometric titration, infrared and nmr spectra.
Riboflavin Tetrabutyrate의 합성에 관한 연구
李英行,李鍾律,李寀浩 圓光大學校 基礎自然科學硏究所 1983 基礎科學硏究誌 Vol.2 No.1
Riboflavin(Vitamin B_2) is a component of two closely related coenzymes, flavin mononucleotide(FMN) and flavin adenine dinucleotide(FAD). Riboflavin tetrabutyrate is more fat-soluble than riboflavin, which is highly absorbed in vivo. and hydrolysed to give riboflavin. Riboflavin tetrabutyrate has always been synthesized by general method of ester. But the use of DMAP was found be very effective for esterification of riboflavin with butyric acid.
Diethyl 3,4,5, - Trimethoxybenzylmalonate의 새로운 합성법
李茶浩,李英行,李晩求,蔡奎允 圓光大學校 1984 論文集 Vol.18 No.2
3,4,5 - Trimethoxybenjoyl chloride 와 diethyl malonate를 축합시키고 이어서 염소화반응 및 수소화반응에 의하여 70%의 수득률로서 diethyl 3,4,5 - trimethoxybenzylmalonate를 얻었다. direct condensation of 3,4,5 - trimethoxybenzoyl chloried with diethyl malonate followed by chlorination and hydrogenation afforded diethyl 3,4,5 - trimethoxybenzylmalonate in 70% overall yield.
N-Isoprophyliminotriphenylphosphorane과 Benzaldehyde 유도체와 반응
李英行,李晩求,金基炫 圓光大學校 基礎自然科學硏究所 1986 基礎科學硏究誌 Vol.5 No.2
The reactions of N- sopropyliminotriphenylphosphorane with benzaldehyde derivatives were investigated by GC. The reaction were completed within 8hours at an approximate reaction condition. The reactivity of benzaldehyde was in order, Ar=p-NO_2>p-Cl>p-Br>H>p-CH_3>p-CH_3O> and Ar=p-C_2H_5O, consistant with the Wittig mechanism. The reactivity of iminophosphorane increased with the change of reaction solvent from benzene to ethanol.
이귀행,박민철,노승호,백영석,이상열,김재현 圓光大學校 醫科學硏究所 1996 圓光醫科學 Vol.12 No.2
Eighteen patients took Moclobemide for 6 weeks, who had been diagnosed as major depression based on DSM-Ⅲ-R and had had more than 16 points on the Hamilton Depression Rating Scale. After medication of Moclobemide, they were evaluated by the Hamilton Depression Rating Scale and in terms of sleep, vigilance, performance, social interactions and drive. The results were as follows ; 1. The average dosage of Moclobemide was 400±89 ㎎. 2. Antidepressant effect were checked on the all items of the Hamilton Depression Rating Scale and prominent on the items of work and activities, insomnia, suicide, somatic symptoms. 3 There were obvious changes of the antidepressive effect by the evaluation of the doctors and patients at 4 weeks after the medication of Moclobemide. 4. In the patients, 61% had positive effects on the sleep. 94% no negative effects on the vigilance. Nobody has negative effects on the social interactions and drive. 5. Side effects or physical disturbances induced by Moclobemide were not found. According to these results, it seemed that Moclobemide had clear antidepressant effects, few negative effects on the life of day time, positive effects on the sleep and somatic symptoms.
전해산성수를 이용한 새로운 내시경 소독 시스템(Cleantop WM-1??)의 소독효율
이준행,이풍렬,송재훈,이남용,임윤정,장재권,김영호,김재준,백승운,이종철,최규완 대한감염학회 2001 감염 Vol.33 No.2
Background : Electrolyzed acid water (EAW) is a new liquid chemical germicide containing a mixture of oxidizing species and prepared by mixing a small amount of salt with tap water in an electrolyzer. We attempted an in-use evaluation of the high-level disinfection capability of Cleantop WM-1□, a new endoscope reprocessing system using EAW. Methods : Forty-seven flexible endoscopes were randomly collected just after upper endoscopic examinations and were disinfected using Cleantop WM-1□. Parts of the endoscopes without contact to EAW were disinfected with 75% ethyl alcohol. Immediately after the disinfection procedure, samples were taken from the biopsy channel (S-1), tip of the insertion tube (S-2), the umbilical cord (S-3), and the angulation knob (S-4). Results : In EAW-disinfected parts of the endoscopes, the culture-positive rates were 4.3% (2/47) in S-1 samples and 12.8% (6/47) in S-2 samples. In ethyl alcohol-disinfected area, the culture-positive rates were 2.1% (1/47) in S-3 samples and 25.5% (12/47) in S-4 samples. The colony counts of culture-positive samples ranged from 1 to 144. Pseudomonas aerugi-nasa was recovered from the angulation knob of an endoscope, but other contaminating organisms were mostly : normal flora or opportunistic pathogens. Conclusion : Although part of the endoscopes disinfected with 75% ethyl alcohol were contaminated with more organisms than EAW-disinfected areas, Cleantop WM-1□ showed a relatively good disinfection efficacy in reprocessing patient-used endoscopes. (Korean J Infect Dis 33:133∼138, 2001)
새로운 의약품의 합성에 관한 연구 : 6-Thiocyanopenicillanic Acid 유도체의 합성
李英行,李寀浩,崔元植 원광대학교기초자연과학연구소 1992 基礎科學硏究誌 Vol.11 No.3
6-Aminopenicillanic acid의 diazo화 반응과 sodium thiocyanate와 반응으로 새로운 β-lactam 화합물인 6-thiocyanopenicillanic acid(1a)를 합성하고 p-nitrobenzyl bromide, chloromelthylpivalate 및 1-chlorodiethylcarbonate들과의 반응에 의해 각각에 해당하는 ester(1b~d)를 합성하였다. A new β-lactam compound, 6-thiocyanopenicillanic acid(1a) was prepared by the reaction of diawnium salt of 6-aminopenicillanic acid with sodium thiocyanate. Reaction of 6-thiocyanopenicillanic acid(la) with p-nitrobenzyl bromide, chloromethylpivalate and l-chlorodiethylcarbonate, respectively, afforded the corresponding esters(1b~d).
李寀浩,李英行 圓光大學校 1982 論文集 Vol.16 No.2
Trimethoprim은 그람음성균과 변형균에 대하여 광범위한 항균력을 가진다. Trimethoprim은 흔히 3,4,5-trimethoxybenzaldelyde를 출발물질로 사용하여 합성되며 그 합성자체가 복잡하고 어려운 점이 많다. 이러한 어려운 점을 피하기 위하여 3,4,5-trimethoxybenzoic acid를 출발물질로 사용하였으며 그의 acid chloride와 ethyl cyanoacetate나 diethyl malonate를 축합시켜서 Trimethoprim의 중간체인 diethyl 3,4,5-trimethoxybenzolymalonate와 diethyl 3,4,5-trimethoxybenzylmalonate를 합성하였다. Trimethoprim has a moderately broad antibacterial spectrum which includes many of the gram-negative species. This compound has always been synthesized starting from 3,4,5-trimethoxy benzaldebyde, but the synthesis of the starting material itself were very complicated and tedious. To avoid these difficulties, we used 3,4,5-trimethoxybenzoic acid as starting material and attempted to condense ethyl cyanoacetate and diethyl malonate with 3,4,5-trimethoxybenzoyl chloride. As a result, the intermediates for the synthesis of trimethoprim, diethyl 3,4,5-trimethoxybenzoylmalonate and diethyl 3,4,5-trimethoxybenzylmalonate were synthesized.