• Bulletin of the Korean Chemical Society
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• 제10권4호
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• pp.382-388
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• 1989

The approximate rates and stoichiometry of the reaction of excess potassium tri-sec-butylborohydride ($K_s-Bu_3BH$) with selected organic compounds containing representative functional groups were determined under the standard conditions (0$^{\circ}C$, THF) in order to define the characteristics of the reagent for selective reductions. Primary alcohols evolve hydrogen in 1 h, but secondary and tertiary alcohols and amines are inert to this reagent. On the other hand, phenols and thiols evolve hydrogen rapidly. Aldehydes and ketones are reduced rapidly and quantitatively to the corresponding alcohols. Reduction of norcamphor gives 99.3% endo- and 0.7% exo-isomer of norboneols. The reagent rapidly reduces cinnamaldehyde to the cinamyl alcohol stage and shows no further uptake of hydride. p-Benzoquinone takes up one hydride rapidly with 0.32 equiv hydrogen evolution and anthraquinone is cleanly reduced to the 9,10-dihydoxyanthracene stage. Carboxylic acids liberate hydrogen rapidly and quantitatively, however further reduction does not occur. Anhydrides utilize 2 equiv of hydride and acyl chlorides are reduced to the corresponding alcohols rapidly. Lactones are reduced to the diol stage rapidly, whereas esters are reduced moderately (3-6 h). Terminal epoxides are rapidly reduced to the more substituted alcohols, but internal epoxides are reduced slowly. Primary and tertiary amides are inert to this reagent and nitriles are reduced very slowly. 1-Nitropropane evolves hydrogen rapidly without reduction and nitrobenzene is reduced to the azoxybenzene stage, whereas azobenzene and azoxybenzene are inert. Cyclohexanone oxime evolves hydrogen without reduction. Phenyl isocyanate utilizes 1 equiv of hydride to proceed to formanilide stage. Pyridine and quinoline are reduced slowly, however pyridine N-oxide takes up 1.5 equiv of hydride in 1 hr. Disulfides are rapidly reduced to the thiol stage, whereas sulfide, sulfoxide, sulfonic acid and sulfone are practically inert to this reagent. Primary alkyl bromide and iodide are reduced rapidly, but primary alkyl chloride, cyclohexyl bromide and cyclohexyl tosylate are reduced slowly.

• 한국환경농학회지
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• 제15권4호
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• pp.501-505
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• 1996

새로운 sulfonamide형(型) 제초제(除草劑) asimsulfuron은 논에서 발생(發生)하는 다년생(多年生) 잡초(雜草)인 너도방동사니, 올방개, 올미, 벗풀 및 올챙고랭이에 대하여 7.5 - 30 g ai/ha 처리(處理) 수준(水準)에서 선택적(選擇的)인 방제(防除) 효과(效果)를 나타낸다. Azimsulfuron 0.3 - 30 ppm 수준(水準)을 포함(包含)한 양액(養液) 재배(栽培)에서 화본과(禾本科)에 대한 내성(耐性) 검정(檢定) 결과(結果), 벼 및 피의 지상부(地上部) 경엽(莖葉)에 대한 저해(沮害)보다는 뿌리에 대하여 더 큰 저해(沮害)를 나타내었다. 그러나 벼의 뿌리는 피에 대하여서 azimsulfuron에 대하여 약 5배(倍) 이상(以上)의 내성(耐性)을 보였다. 올챙고랭이 생육(生育) 50% 저해(沮害)에 필요(必要)한 농도(濃度)를 기준(基準)으로 측정(測定)한 토양(土壤) 중(中) 하방(下方) 이동(移動)은 3일간(日間) 3 cm/일(日)의 용탈(溶脫) 조건하(條件下) $20^{\circ}C$ 및 $30^{\circ}C$에서 배양(培養)된 azimsulfuron의 잔효성(殘效性)은 각각 30일(日) 및 21일(日) 지속(持續)되었다. Azimsulfuron 15 g ai/ha 처리(處理) 후(後) 3일(日) 동안 3 cm/일(日) 용탈(溶脫)시킨 토양(土壤)컬럼에서 표층(表層) 하(下) 5, 10 및 15 cm에 이식(移植)된 벗풀의 건물중(乾物重)은 각 층위(層位)에서 출아(出芽)된 무처리(無處理) 대비(對比) 87%, 85% 및 79%로써 azimsulfuron에 대한 벗풀의 감수성(感受性)은 이식(移植) 심도(深度)에 따라 크게 변하지 않았다.

• Journal of Plant Biotechnology
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• 제47권1호
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• pp.100-106
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• 2020

Coix lacryma-jobi (Hanjeli) is known to posses anti-microbial properties. Therefore, phytochemical compounds of C. lacryma-jobi have been studied to produce novel antimicrobial agents as treatments against antibiotic-resistant bacteria.The objective of this study was to determine the phytochemical composition and antibacterial activity of the C. lacryma-jobi oil against Escherichia coli, Staphylococcus aureus, and Bacillus subtilis. The phytochemical composition of the oil was determined via gas chromatography mass spectrophotometry (GC-MS). Moreover, agar disk and agar well diffusion were employed to screen the antibacterial activity of the oil. An agar well diffusion test was implemented to determinate MIC's (minimum inhibitory concentrations). Dodecanoic acid, tetradecanoic acid, 2,3-dihydroxypropylester, 1,3-dioctanoin, N-methoxy-N-methyl-3,4-dihydro-2H-thiopyran6-carboxamide, propanamide, 5-Amino-1-(quinolin-8-yl)-1,2,3-triazole-4-carboxamide, and pyridine were identified in the C. lacryma-jobi oil. The MIC value of the oil was 0.031 g/L and the MBC of the oil was 0.125 g/L effective in all test bacteria. Dodecanoic acid displayed inhibitory activity against gram-positive and gram-negative bacteria. Therefore, our research demonstrated C. lacryma-jobi (Hanjeli) oil exhibited antibacterial activity against E. coli, S. aureus, and B. subtilis. These research suggest that C. lacryma-jobi root oil could be used for medicinal purposes; however clinical and in vivo tests must be performed to evaluate its potential as an antibacterial agent.

• 연구논문집
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• 통권27호
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• pp.101-108
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• 1997

The characteristics of combustion and emissions in multi-staged oil burner have been experimentally studied for the various range of equivalence ratios, drop sizes and fuel formulations. Malvern system was used to measure droplet size of fuel. Light fuel oil and light fuel oil doped with pyridine($C_5H _5N$) were used to investigate the effects on fuel NOx emission. The emissions of NO and CO in exhaust gas and the flame temperatures were measured by the gas analyzer and thennocouples. NOx emissions were increased by increasing the excess air ratio (range:$lambda=1.1-1.4$) or decreasing the SMD of droplet in single-staged burner. In comparison with the single-staged burner, the emission of NOx in multi-staged burner was reduced by 50% but CO emission was slightly increased. It is found that multi-staged burner has a good capability in reducing thermal NOx resulting from the distributed heat release rate and lower flame temperature in fuel-rich and fuel-lean combustion zone. Moreover, the fuel NOx emission of the multi-staged burner is lower than that of single-staged burner, because multi-staged burner has fuel rich zone where fuel N is converted to $N_2$ more than NO. In 3-staged burner, the percentage of each stage combustion air have strong influence on emission characteristics. It is also found that NOx emission can be reduced by decreasing inner and outer air percentage or increasing middle air flow rate and CO emission is vice versa.

• Applied Biological Chemistry
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• 제13권1호
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• pp.65-72
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• 1970

Bence Jones 단백질중(蛋白質中) ${\lambda}$형(型)의 N-말단(末端) 및 그 주변(周邊)의 아미노산배열(酸配列)을 결정(決定)하기 위하여 본(本) 실험(實輸)이 시도(試圖)되었던바 그 결과(結果)는 다음과 같다. 1) Bence Jones 단백질(蛋白質)을 Pronase와 Chymotrypsin으로 분해(分解)하여 얻은 Peptide중에서 Im Pr-M 및 Im Ch-M와 Ik Ch-M을 Dowex $50{\times}2$ column $1{\times}20$cm)와 Dowex $1{\times}2$ column $(0.9{\times}50{\;}cm)$을 사용(使用)하여 분리(分離)하였다. 2) ${\lambda}$형(型) Bence Jones단백질(蛋白質)의 N-말단(末端)은pyrroglutamic acid로 되어 있음을 alkali반응(反應)과 고압여지전기영동법(高壓濾紙電氣泳動法)으로 확인(確認)하였다. 3) 농염산(濃鹽酸)(12N) 반응(反應)($27^{\circ}C$, 15시간(時間))을 이용(利用)하며 Peptide중(中)의 Serine부(部)를 선택적(選擇的)으로 절단(切斷)할 수 있었다. 4) 이들 Peptide의 아미노배열순서(配列順序)는 Edman의 PTC법(法)과 소거법(消去法) 및 CarboBypeptidase A를 사용(使用)하여 결정(決定)하였다. 5) 분리(分離)한 Peptide의 아미노산배열순서(酸配列順序)는 다음과 같았다. $Im\;Ch-M\;PCA{\cdot}Ser{\cdot}Val{\cdot}Leu$ $Ik\;Ch-M\;PCA{\cdot}Ser{\cdot}Ala{\cdot}Leu1$