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黄烷酮衍生物的合成及杀菌活性 被引量:2

Synthesis and Fungicidal Activity of Flavanone Derivaties
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摘要 以取代苯甲醛为起始原料 ,经过肉桂酸衍生物合成了 7个黄烷酮衍生物 ,它们的结构分别经IR和1 H NMR确证。通过生物测试表明 。 Seven flavanone derivaties were synthesized.Their structures were confirmed by IR and 1HNMR.It is found from biological examination that some of these compounds have good fungicidal activity.
出处 《湖北化工》 2002年第3期24-25,共2页 Hubei Chemical Industry
基金 湖北省自然科学基金 (99J0 59)资助项目
关键词 衍生物 黄烷酮 合成 杀菌活性 flavanone synthesis fungicidal activity
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  • 1陈俊杰,厦门大学学报,1992年,31卷,1期,106页
  • 2KodamaO,LiWX,TamogamiS,etal.OryzalexinS,ANovelStemarace-typeDiterpeneRicePhytoalexin.BiosciBiotechBiochem,1992,56:1002.
  • 3KodamaO,MiyakawaJ,AkatsukaT,etal.Sakuranetin,AFlavanonePhytoalexinFromUltraviolet-IrradiatedRiceLeaves.Phytochemistry,1992,31:3807.
  • 4MARKCush-man,DhanapalanNagarathnam.SynthesisandProtein-TyrosineKinaseInhibitoryActivitiveofFlavonoidAualogues.rMedChem,1991,34:798-806.
  • 5CHENGTie-min,WANGYuan,CUIMeng-sheng.StudiesonAzaflavonoids.OrganicChemistry,1988,8:250-253(Ch).
  • 6ChhabraSC,GupiaSR.Synthesisof5,7,3',4'-Tetrehydroxy-8-methoxyflavone.IndianJChem,1978,16:1079-1080.
  • 7CHENJun-jie,YANGWei-wen,PANXin-fu,etal.ANovelSynthesisofFlavanones.ChemicalJournalofChineseUnivesities,1987,8:914-916(Ch).
  • 8LITian-quan.FundamentalsofOrganicSynthesis.Beijing:HigherEdncationalPress,1992.85-91.
  • 9WANGYan-gong.AnIntroductionToModernOrganicSynthesis.Wuhan:CentralChinaNormalUniversityPress,1995.201-205(Ch).

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  • 1Achenbach H, Stoecher M, Constenla M A. Constituents of tropical medicinal plants. Part 31. Flavonoid and other constituents of Bauhinia manca[J]. Phytochemistry, 1988,27 (6) : 1835.
  • 2Wollenweber E, Seigler D S. Flavonoids from the exudate of Acacia neovernlcosa[J]. Phytochemistry, 1982,21(5):1063.
  • 3Matthias O H, Geoffrey A C, Payom T, et al. Traditional medicinal plants of Thailand, Ⅷ. Isoflavonoids of Dalbergia candenatensis[J]. J Nat P, 1987,50(4) :696.
  • 4Tanaka T, Linuma M, Yuki K, et al. Flavonoids in root bark of Pongamia pinnata[J]. Phytochemistry, 1992,31 (3) :993.
  • 5Grogso M, Ollis W D, Redman B T, et al. Neoflavonoid group of natural products. Part 8. Obtusastyrene and obtustyrene, cinnamylphenols from Dalbergia retusa[ J ]. Phytochemistry, 1978,17(8) :1395.
  • 6Krasnov E A, Ermilova E V, Kadyrova T V, et al. Phenolic components of Empetrum nigrum extract and the crystal structure of one of them[J]. Chem Nat Compd, 2000,36(5) :493.
  • 7YAMAMOTO C,OKAMOTO Y. Optically active polymers for chiral separation [ J ]. Bull Chem. Soc. , 2004,77 ( 6 ) : 227 -257.
  • 8ZHOU Zhi-qiang,TIAN Qin, LV Chun-guang, et al. Direct enantiomeric separation of chiral pesticides by LC on am- ylose tris ( 3, 5-dimethylphenylcarbamate ) stationary phase under reversed phase conditions [ J ]. Chroma- tographia, 2010,71 ( 9 ) : 855 -865.
  • 9YAMAMOTO C, HAYASHI T, OKAMOTO Y, et al. Di- rect resolution of C76 enantiomers by HPLC using an am- ylose-based chiral stationary phase[ J]. Chem. Commun. , 2001,17( 1 ) :925-926.
  • 10TANG S, IKAI T, TSUJI M, et al. Immobilization and chiral recognition of 3, 5-dimethylphenylcarbamates of cellulose and amylosebearing 4-(trimethoxysilyl) phenyl- carbamate groups [ J ]. Chirality, 2010,22 ( 1 ) : 165-172.

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