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      Alkylphenyl fluorobenzoate 유도체들의 합성과 몇 가지 식물병원균에 대한 항균활성 = A Synthesis of Alkylphenyl fluorobenzoate Derivatives and Their Antifungal Activities on Several Phytopathogens

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      https://www.riss.kr/link?id=A104682988

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      국문 초록 (Abstract) kakao i 다국어 번역

      Thymol(I), 5-isopropyl-3-methylphenol(II), 4-isopropyl-3-methylphenol(III), 2-sec-butylphenol(IV)과 4-sec- butylphenol(V)을 출발물질로 하여 alkylphenyl fluorobenzoate계 ester 유도체 60종을 합성하였다. 이 유도체들의 합성은 IR, 1H-NMR과 GC/MS를 이용하여 확인하였다. 이들 화합물들에 대하여 토마토 역병균, 오이 잿빛곰팡이병균, 오이 탄저병균과 벼 잎집무늬마름병균에 대한 항균활성을 조사하였다. 오이 잿빛곰팡이병균에 2-sec-butylphenyl 2,5-difluorobenzoate (IV-6)와 4-sec-butylphenyl 2,5-difluorobenzoate(V-6)등이 90% 이상의 우수한 항균활성을 나타내었다. 오이 탄저병균에 대하여 2-isopropyl-5-methylphenyl 2,3,6-trifluorobenzoate(I-11), 2-isopropyl-5-methylphenyl 2,4,5-trifluorobenzoate(I-12), 5-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate(II-11), 4-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate(III-11)와 4-isopropyl-3-methylphenyl 2,4,5-trifluorobenzoate(III-12)가 90% 이상의 매우 우수한 항균활성을 나타내었다.
      번역하기

      Thymol(I), 5-isopropyl-3-methylphenol(II), 4-isopropyl-3-methylphenol(III), 2-sec-butylphenol(IV)과 4-sec- butylphenol(V)을 출발물질로 하여 alkylphenyl fluorobenzoate계 ester 유도체 60종을 합성하였다. 이 유도체들의 합성은 ...

      Thymol(I), 5-isopropyl-3-methylphenol(II), 4-isopropyl-3-methylphenol(III), 2-sec-butylphenol(IV)과 4-sec- butylphenol(V)을 출발물질로 하여 alkylphenyl fluorobenzoate계 ester 유도체 60종을 합성하였다. 이 유도체들의 합성은 IR, 1H-NMR과 GC/MS를 이용하여 확인하였다. 이들 화합물들에 대하여 토마토 역병균, 오이 잿빛곰팡이병균, 오이 탄저병균과 벼 잎집무늬마름병균에 대한 항균활성을 조사하였다. 오이 잿빛곰팡이병균에 2-sec-butylphenyl 2,5-difluorobenzoate (IV-6)와 4-sec-butylphenyl 2,5-difluorobenzoate(V-6)등이 90% 이상의 우수한 항균활성을 나타내었다. 오이 탄저병균에 대하여 2-isopropyl-5-methylphenyl 2,3,6-trifluorobenzoate(I-11), 2-isopropyl-5-methylphenyl 2,4,5-trifluorobenzoate(I-12), 5-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate(II-11), 4-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate(III-11)와 4-isopropyl-3-methylphenyl 2,4,5-trifluorobenzoate(III-12)가 90% 이상의 매우 우수한 항균활성을 나타내었다.

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Sixty compounds such as alkylphenyl fluorobenzoate esters from thymol(I), 5-isopropyl-3-methylphenol (II), 4-isopropyl-3-methylphenol (III), 2-sec-butylphenol (IV) and 4-sec-butylphenol (V) were synthesized. These derivatives were identified by IR, 1H-NMR spectrometer and GC/MS. Their in vivo antifungal activities were tested against phytopathogens such as Phytophthora infestans, Botrytis cinerea, Colletotrichum orbiculare and Rhizoctonia solani. As the result, 2-sec-butylphenyl 2,5-difluorobenzoate (IV-6) and 4-sec-butylphenyl 2,5- difluorobenzoate (V-6) showed 90% above antifungal activity against Botrytis cinerea. 2-Isopropyl-5-methylphenyl 2,3,6-trifluorobenzoate (I-11), 2-isopropyl-5-methylphenyl 2,4,5-trifluorobenzoate (I-12), 5-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate (II-11), 4-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate (III-11) and 4-isopropyl-3- methylphenyl 2,4,5-trifluorobenzoate (III-12) showed 90% above potent antifungal activity against Colletotrichum orbiculare.
      번역하기

      Sixty compounds such as alkylphenyl fluorobenzoate esters from thymol(I), 5-isopropyl-3-methylphenol (II), 4-isopropyl-3-methylphenol (III), 2-sec-butylphenol (IV) and 4-sec-butylphenol (V) were synthesized. These derivatives were identified by IR, 1H...

      Sixty compounds such as alkylphenyl fluorobenzoate esters from thymol(I), 5-isopropyl-3-methylphenol (II), 4-isopropyl-3-methylphenol (III), 2-sec-butylphenol (IV) and 4-sec-butylphenol (V) were synthesized. These derivatives were identified by IR, 1H-NMR spectrometer and GC/MS. Their in vivo antifungal activities were tested against phytopathogens such as Phytophthora infestans, Botrytis cinerea, Colletotrichum orbiculare and Rhizoctonia solani. As the result, 2-sec-butylphenyl 2,5-difluorobenzoate (IV-6) and 4-sec-butylphenyl 2,5- difluorobenzoate (V-6) showed 90% above antifungal activity against Botrytis cinerea. 2-Isopropyl-5-methylphenyl 2,3,6-trifluorobenzoate (I-11), 2-isopropyl-5-methylphenyl 2,4,5-trifluorobenzoate (I-12), 5-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate (II-11), 4-isopropyl-3-methylphenyl 2,3,6-trifluorobenzoate (III-11) and 4-isopropyl-3- methylphenyl 2,4,5-trifluorobenzoate (III-12) showed 90% above potent antifungal activity against Colletotrichum orbiculare.

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      참고문헌 (Reference)

      1 최원식, "식물오일과 그 성분들의 살균활성" 한국농약과학회 10 (10): 201-209, 2006

      2 최원식, "Thymol과 Carvacrol 유도체들의 합성과 식물병원균에 대한 항균활성" 한국농약과학회 10 (10): 237-248, 2006

      3 Lee, S. E., "Suppression of ochratoxin biosynthesis by naturally occurring alkaloids" 24 (24): 391-397, 2007

      4 Lewis, R. J., "Sax’s Dangerous Properties of Industrial Materials. 8th Ed." Van Nostrand-Reinhold 1992

      5 Lee, B. H., "New Formulations of Ethyl Formate to Control Internal Stages of Sitophilus oryzae" 10 (10): 369-374, 2007

      6 최원식, "Isopropylphenyl 유도체들의 합성과 식물병원균에 대한 항균활성" 한국응용생명화학회 50 (50): 178-186, 2007

      7 Lee, S. E., "Inhibitory Effect on Aflatoxin B1-8,9-epoxide Formation and Anti-complementary Activity of Methanol Extract from Hericium erinaceus Cultivated with Artemisia iwayomogi" 12 (12): 183-186, 2003

      8 Lee, B. H., "Fumigant toxicity of essential oils from the Myrtaceae family and 1, 8-cineole against 3 major stored-grain insects" 40 : 553-564, 2004

      9 Choi, W. S., "Fumigant toxicity of essential oils and monoterpens against Lycoriella mali adults" 25 : 398-401, 2006

      10 Ormancey, X., "Formulation of essential oils in functional perfumery" 157 : 30-40, 2001

      1 최원식, "식물오일과 그 성분들의 살균활성" 한국농약과학회 10 (10): 201-209, 2006

      2 최원식, "Thymol과 Carvacrol 유도체들의 합성과 식물병원균에 대한 항균활성" 한국농약과학회 10 (10): 237-248, 2006

      3 Lee, S. E., "Suppression of ochratoxin biosynthesis by naturally occurring alkaloids" 24 (24): 391-397, 2007

      4 Lewis, R. J., "Sax’s Dangerous Properties of Industrial Materials. 8th Ed." Van Nostrand-Reinhold 1992

      5 Lee, B. H., "New Formulations of Ethyl Formate to Control Internal Stages of Sitophilus oryzae" 10 (10): 369-374, 2007

      6 최원식, "Isopropylphenyl 유도체들의 합성과 식물병원균에 대한 항균활성" 한국응용생명화학회 50 (50): 178-186, 2007

      7 Lee, S. E., "Inhibitory Effect on Aflatoxin B1-8,9-epoxide Formation and Anti-complementary Activity of Methanol Extract from Hericium erinaceus Cultivated with Artemisia iwayomogi" 12 (12): 183-186, 2003

      8 Lee, B. H., "Fumigant toxicity of essential oils from the Myrtaceae family and 1, 8-cineole against 3 major stored-grain insects" 40 : 553-564, 2004

      9 Choi, W. S., "Fumigant toxicity of essential oils and monoterpens against Lycoriella mali adults" 25 : 398-401, 2006

      10 Ormancey, X., "Formulation of essential oils in functional perfumery" 157 : 30-40, 2001

      11 Kumar, R., "Evaluation of some essential oils as botanical fungitoxicants for the protection of stored food commodities from fungal infestation" 87 : 1737-1742, 2007

      12 Szczebanik, M., "Essential oil vapours control some commom postharvest fungal pathogens" 47 : 103-109, 2007

      13 Nychas, G. E., "Encyclopedia of food microbiology in : Traditional preservatives- oils and spices" Academic press 1717-1722, 2000

      14 Vina, W. Yang, "Antifungal effect of essential oils on southern yellow pine" 59 : 302-306, 2007

      15 최원식, "4-isopropyl, 5-isopropyl-3-methylphenol 유도체들의 합성과 식물병원균에 대한 항균활성" 10 (10): 249-261, 2006

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      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2006-01-01 평가 신청제한 (등재후보1차)
      2005-01-01 평가 등재후보학술지 유지 (등재후보2차) KCI등재후보
      2004-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2003-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      2016 0.42 0.42 0.41
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