SYNTHESES OF 2,4,6-TRIHYDROXY-, 2,4,6-TRIHYDROXY-5-METHYL- AND 2,4,5,6-TETRAHYDROXY-SUBSTITUTED 3-(3-PHENYLPROPIONYL)BENZALDEHYDES AND THEIR BACTERICIDAL ACTIVITY

Sato S; Obara H; Takeuchi H; Tawaraya T; Endo A; Onodera JI

首页> 外文期刊>Phytochemistry >SYNTHESES OF 2,4,6-TRIHYDROXY-, 2,4,6-TRIHYDROXY-5-METHYL- AND 2,4,5,6-TETRAHYDROXY-SUBSTITUTED 3-(3-PHENYLPROPIONYL)BENZALDEHYDES AND THEIR BACTERICIDAL ACTIVITY

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SYNTHESES OF 2,4,6-TRIHYDROXY-, 2,4,6-TRIHYDROXY-5-METHYL- AND 2,4,5,6-TETRAHYDROXY-SUBSTITUTED 3-(3-PHENYLPROPIONYL)BENZALDEHYDES AND THEIR BACTERICIDAL ACTIVITY

机译：2,4,6-三羟基-，2,4,6-三羟基-5-甲基-和2,4,5,6-四羟基取代的3-（3-苯丙基）苯并二氢的合成及其杀菌活性

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摘要

2,4,6-Trihydroxy-, 2,4,6-trihydroxy-5-methyl-, and 2,4,5,6-tetrahydroxy-substituted 3-(3-phenylpropionyl) benzaldehydes were efficiently synthesized. The first two compounds showed bactericidal activity for Pseudoperonospora cubersis.

机译：有效地合成了2,4,6-三羟基-，2,4,6-三羟基-5-甲基-和2,4,5,6-四羟基取代的3-（3-苯基丙酰基）苯甲醛。前两种化合物显示对立方假单胞菌的杀菌活性。

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来源
《Phytochemistry》 |1995年第2期|共3页
作者
Sato S; Obara H; Takeuchi H; Tawaraya T; Endo A; Onodera JI;
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正文语种 eng
中图分类植物生物化学;
关键词
Antifungal activity; Antifeedant activity; Bactericidal activity;

机译：抗真菌活性;拒食活性;杀菌活性;

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专利

1. SYNTHESES OF 2,4,6-TRIHYDROXY-, 2,4,6-TRIHYDROXY-5-METHYL- AND 2,4,5,6-TETRAHYDROXY-SUBSTITUTED 3-(3-PHENYLPROPIONYL)BENZALDEHYDES AND THEIR BACTERICIDAL ACTIVITY [J] . Sato S, Obara H, Takeuchi H, Phytochemistry . 1995,第2期

机译：2,4,6-三羟基-，2,4,6-三羟基-5-甲基-和2,4,5,6-四羟基取代的3-（3-苯丙基）苯并二氢的合成及其杀菌活性
2. Syntheses and ~1H NMR spectra of substituted zintl ions [Ge _9R_n]~((4-n)-): Crystal structures of [Ge _9R]~(3-) (R = 2,4,6-Me_3C_6H_2, CHCH_2) and indication of tris-vinylated clusters [J] . Benda C.B., Wang J.-Q., Wahl B., European journal of inorganic chemistry . 2011,第27期

机译：取代的zintl离子[Ge _9R_n]〜（（4-n）-）的合成和〜1H NMR光谱：[Ge _9R]〜（3-）的晶体结构（R = 2,4,6-Me_3C_6H_2，CHCH_2）和三乙烯基化簇的指示
3. Syntheses and Reactions of Halo- and Arylazo-Substituted 3-(3-(2-Naphthyl)acryloyl)tropolones: Formation of (Naphthalen2-yl)Vinyl)-Substituted Heterocycle-Fused Troponoid Compounds [J] . Gao WT, Sun MC, Li Y, Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry . 2009,第6期

机译：卤代和芳基偶氮取代的3-（3-（2-（萘基）丙烯酰基）对羟基苯甲酸酯的合成与反应：（萘基-2-基）乙烯基）取代的杂环融合类风湿化合物的形成
4. Syntheses, Structure and Herbicidal Activity of Substituted Phenyl Pyrazole Derivatives [C] . The 12th Asian Pacific Confederation of Chemical Engineering Congress(第十二届亚太化工联盟大会暨化工展览会)论文集 . 2008

机译：取代的苯基吡唑衍生物的合成，结构和除草活性
5. I. A1,3- strain enabled retention of chirality during Bis-cyclization of β-ketoamides: Asymmetric synthesis and bioactivity of salinosporamide a and derivatives II. Optimization of an Organic syntheses procedure: asymmetric nucleophile-catalyzed aldol-lactonization with aldehyde acids [D] . Nguyen, Henry 2010

机译：I. A1,3-菌株能够在β-酮基酰胺的双环化过程中保留手性：salinosporamide a和衍生物II的不对称合成和生物活性。有机合成程序的优化：醛酸不对称亲核催化醛醇内酯化
6. Syntheses of 3-(Alkylamino)methylene-6-methylpyridine-24(1H3H)-diones 3-Substituted 7-Methyl-2H-pyrano32-cpyridine-25(6H)-dione Fluorescence Probes and Tetrahydro-1H9H-210-dioxa-9-azaanthracen-1-ones [O] . Allan M. Prior, Medha J. Gunaratna, Daisuke Kikuchi, -1

机译：3-（烷基氨基）亚甲基 -6-甲基吡啶-24（1H3H）-二酮的合成3-取代的7-甲基-2H-吡喃并32-c吡啶-25（6H））-二酮荧光探针和Tetrahydro-1H9H-210-dioxa-9-azaanthracen-1-ones
7. Studies on the Synthesis of Analgesics. LIV. Syntheses of 3-(Substituted phenyl)-4-oxazolidinone and 3-(Substituted phenyl)-3, 4, 5, 6-tetrahydro-2H-1, 3-oxazin-4-one Derivatives as Analgesics (Studies on the Syntheses of Heterocyclic Compounds. CMXXVIII) [O] . TETSUJI KAMETANI, KAZUO KIGASAWA, MINEHARU HIIRAGI, 1981

机译：镇痛药合成研究。 LIV。合成的3-（取代的苯基）-4-恶唑烷酮和3-（取代的苯基）-3,4,5,6-四羟基-2H-1,3-恶化-4-一种衍生物作为镇痛药（关于合成的研究杂环化合物。CMXXVIII）

SYNTHESES OF 2,4,6-TRIHYDROXY-, 2,4,6-TRIHYDROXY-5-METHYL- AND 2,4,5,6-TETRAHYDROXY-SUBSTITUTED 3-(3-PHENYLPROPIONYL)BENZALDEHYDES AND THEIR BACTERICIDAL ACTIVITY

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