• 제목/요약/키워드: derivative synthesis

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Ricinine 유도체(誘導體)의 합성(合成) 및 농약활성(農藥活性) (Synthesis and pesticidal activity of ricinine derivatives)

  • 권오경;임수길;홍수명;이성은;경석헌
    • 농약과학회지
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    • 제2권1호
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    • pp.24-31
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    • 1998
  • 천연물기원 신농약 개발을 위해 유용 식물자원 탐색 및 활성물질의 분리, 동정 결과 벼멸구 살충활성이 높고 분자구조상 유기합성이 용이한 것으로 판단되는 피마자잎중 활성물질 ricinine의 유도체 합성을 통해 고활성 화합물을 얻고자 하였다. 합성된 ricinine을 선도물질로 하여 활성을 증진하고자 분자구조 유사화합물을 비롯한 카바메이트계, 유기인계 화합물 12종을 합성하였다. 카바메이트계 유도체 합성시 전구물질의 pyridine 구조중 carbo기가 있는 chlororicinic acid, ricinic acid는 공명구조가 파괴되어 methyl isocyanate와 반응이 이루어지지 않았다. 유기인계 유도체의 경우 P에 O와 S가 결합된 oxon과 thiono형의 유도체를 합성한 결과 합성수율은 oxon형이 65% 이상인 반면에 thiono형은 20% 미만으로서 낮은 수율을 보였다. 합성 유도체의 생리활성 평가에 있어 유기인계 유도체는 oxon형보다 thiono형 화합물이 높은 살충효과를 나타냈다. Thiono형 유도체는 500 ${\mu}g/ml$ 수준에서 벼멸구에 대한 살충력이 모두 100%이었으며 점박이응애의 경우 특이적으로 thiono형 유도체중 alkyl기의 부분이 methyl인 경우 높은 활성을 나타냈다. Oxon형 유도체, 분자구조 유사화합물과 카바메이트계 유도체의 경우에는 살충력이 나타나지 않았다. 살균 활성은 pyridine ring의 2번 위치에 $NH_{2}$기가 있는 유도체의 경우 200 ${\mu}g/ml$ 수준의 실내검정에서 10종 병원균에 대해 $85{\sim}100%$의 생장저지효과를 보여주었으며, 온실검정에서도 250 ${\mu}g/ml$ 수준에서 벼도열병과 보리흰가루병에 대해 각각 92%, 86%의 방제효과를 나타냈다.

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Synthesis and Characterization of Oligothiophene Derivative

  • Kim, Hyung-Sun;Park, Jong-Won;Ahn, Jun-Hwan;Kim, Yun-Hi;Kwon, Soon-Ki;Do, Lee-Mi
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
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    • pp.665-668
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    • 2004
  • Oligothiophene derivatives have been well-known as an p-type channel material.$^1$ Here, we report novel oligothiophene derivative containing methylene linkage as an p-type channel material. Oligothiophene derivative containing methylene linkage BHTM was synthesized and characterized. BHTM was prepared by a palladium-catalyzed cross-coupling reaction via zinc-substituted thiophene. BHTM exhibited high thermal stability and at least one transition temperature.

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Synthesis and Characterizations of Bis-Spiropyran Derivatives

  • Lee, Sungmin;Ji, Seungwook;Kang, Youngjong
    • Bulletin of the Korean Chemical Society
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    • 제33권11호
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    • pp.3740-3744
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    • 2012
  • We synthesized three different derivatives of bis-spiropyran using simple organic reactions with high yields. BSP1, a derivative of bis-spiropyran having a connection at the position 6' and BSP2, a derivative of bis-spiropyran having a connection at the position 5 and BSP3, a derivative of bis-spiropyran containing a dithienylethene group between two spiropyran moieties were synthesized. The optical properties of BSPs were characterized. UV-Vis spectra showed that BSPs exhibit reversible photo-isomerization and the efficiency of photo-isomerization is highly dependent on the position of nitro group. BSPs having nitro group at para position of hydroxy group showed the higher efficiency of photo-isomerization that the one having nitro group at ortho position. The optical microscope images obtained under ultraviolet or visible light exposure demonstrated that the formation of nanorods can be reversibly controlled by optical signal.

Synthesis of Some New Condensed Pyrimidine Derivatives

  • Mohamed, Enaiat K.;Shehab, Wesam S.
    • 대한화학회지
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    • 제55권6호
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    • pp.988-993
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    • 2011
  • Cyclodehydration of 6-amino-5-cyano pyrimidine derivative (2) afforded pyrimidoisoindole derivatives (3). Compound (3) reacted with carbethoxymethylene derivative to give pyridopyrimidine derivatives (5a,b). Compound (3) was also reacted with formamide to give the corresponding pyrimidopyrimdine derivatives (6) that condensed with benzaldehyde to give Schiff's base (7). Refluxing of compound (3) with triethyl orthoformate afforded compound (8) that cyclized with ammonium hydroxide giving the same compound (6). Compound (8) cyclized with hydrazine hydrate giving compound (9) which also cyclized with triethyl orthoformate affording compound (10). Diazotization of compound (3) led to the formation of triazinopyrimidine derivative (11). Cyclization of compound (11) upon treatment with hydrazine hydrate afforded compound (12). Compound (15) was prepared from reaction of compound (3) and ethylenediamine in presence of carbon disulfide. The behaviour of compound (15) toward benzoyl chloride, triethyl orthoformate, nitrous acid and/or carbon disulfide was also described. All proposed structures were supported by elemental analyses, spectroscopic data and some of the new products showed antimicrobial activity.

Control of the pressurized water nuclear reactors power using optimized proportional-integral-derivative controller with particle swarm optimization algorithm

  • Mousakazemi, Seyed Mohammad Hossein;Ayoobian, Navid;Ansarifar, Gholam Reza
    • Nuclear Engineering and Technology
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    • 제50권6호
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    • pp.877-885
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    • 2018
  • Various controllers such as proportional-integral-derivative (PID) controllers have been designed and optimized for load-following issues in nuclear reactors. To achieve high performance, gain tuning is of great importance in PID controllers. In this work, gains of a PID controller are optimized for power-level control of a typical pressurized water reactor using particle swarm optimization (PSO) algorithm. The point kinetic is used as a reactor power model. In PSO, the objective (cost) function defined by decision variables including overshoot, settling time, and stabilization time (stability condition) must be minimized (optimized). Stability condition is guaranteed by Lyapunov synthesis. The simulation results demonstrated good stability and high performance of the closed-loop PSO-PID controller to response power demand.

Oxalylchloride를 이용한 Sulfonylurea계 유도체 합성에 관한 연구 (Synthesis of Sulfonylurea Derivatives by Oxalylchloride)

  • 경석헌;탁윤흥
    • 한국환경농학회지
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    • 제8권2호
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    • pp.136-141
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    • 1989
  • Sulfonylurea계 화합물의 합성에 필요한 sulfonylisocyanate는 sulfonamide에 $COCl_2$를 반응시켜 얻는 것이 보통이나 본 실험에서는 oxalylchloride를 phosgen 대신 이용하여 sulfonyloxamoylchloride를 합성하고 이것을 열분해하여 얻었다. 이렇게 하여 얻는 sulfonylisocyanate는 각종 아민과 반응하여 높은 수율로 sulfonylurea를 생성하였다.

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아드리아마이신의 유사제제 합성 (1) -안트라싸이클리논의 Isostere 로서 Tetrahydrobenzo(b)phenazine 유도체의 합성- (Synthesis of Adriamycin-related System (1) -Synthesis of the Derivative of Tetrahydrobenzo(b)phenazine as a Potential Isostere of Anthracyclinone-)

  • 장영동;장선영
    • 약학회지
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    • 제34권4호
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    • pp.219-223
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    • 1990
  • 7,8-Dihydro-6,11-dihydroxy-9(10H)benzo(b)phenazinone was prepared from 1,2,3,4-tetra-hydrophenazine as a potential isostere of anthracyclinone. The attempts to functionalize at $C_9$ were not successful due to the unstability of the above ketone.

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Glycyl Norfloxacin 유도체의 합성과 항균작용 (Synthesis and Antimicrobial Activity of Glycyl Norfloxacin Derivatives)

  • 이현수;임채욱;임철부
    • 약학회지
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    • 제43권4호
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    • pp.442-446
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    • 1999
  • The synthesis and antimicrobial activity of N-substituted glycyl derivatives of Norfloxacin were described. Norfloxacin was treated with chloroacetyl chloride to yield chloroacetyl norfloxacin (1). This compounds was treated with alkylamines to obtain quinolone carboxylic acids (2-6), which were reacted with pivaloyloxymethyl chloride to get pivaloyloxymethyl quinolone carboxylates (7-11). Free carboxylic quinolones (2-6) showed little stronger activities to their pivaloyloxymethyl esters (7-11). In quinolone analogues, longer alkyl chain compounds showed stronger activities than shorter one.

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Synthesis and Electroluminescent Properties of Fluoranthene Derivatives

  • Kim, Soo-Kang;Park, Jong-Wook
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2007년도 7th International Meeting on Information Display 제7권1호
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    • pp.621-624
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    • 2007
  • As a new fluoranthene derivative, a synthesis of benzo[k]fluoranthene was suggested, so new blue emitting materials, 7,12-diphenylbenzo[k] fluoranthene [DPBF] and 7,8,10- triphenylfluoranthene [TPF] were synthesized. $EL_{max}$ wavelength of the device using DPBF as an emitting layer was 436 and 454nm in the deepblue region, which are similar values with PL. The device that used DPBF as an emitting layer showed high efficiency of 2.11cd/A and the excellent color coordinate value of (0.161, 0.131) in deep-blue region.

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Synthesis and Biological Evaluation of Decursin, Prantschimgin and Their Derivatives

  • Xia, Yan;Min, Kyung-Hoon;Lee, Kyeong
    • Bulletin of the Korean Chemical Society
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    • 제30권1호
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    • pp.43-48
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    • 2009
  • The synthesis of coumarin-based natural products and their derivatives is described. In vitro MDR reversal activities of the synthesized compounds were evaluated in P-glycoprotein over-expressing human sarcoma cell line MES-SA/DX5. Some of the coumarin derivatives were found to show potent MDR reversal activity. In particular, pyridyl derivative (15e) exhibited more potency than verapamil.