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A series of 3-(N-hydroxylamino)-1,3-diarylpropan-1-one oximes have been synthesized through the reaction of chalcones and hydroxylamine hydrochloride in 56–96% yield within 2–3 h in the presence of sodium acetate in EtOH under ultrasound irradiation. 相似文献
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超声技术在查尔酮合成中的应用研究 总被引:10,自引:0,他引:10
查尔酮是重要的有机合成中间体。报道了在KF-Al2O3的催化下,应用超声波 技术合成查尔酮类化合物的方法,并研究了超声辐射功率、辐射时间对产物产率的 影响,得出了最佳的合成反应条件。控制超声功率为250W,反应30min,查尔酮( 除化合物3b)的产率达95%以上。结果表明该方法操作简单、条件温和、反应速度 快、产率高。 相似文献
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新型1,5-二苯基-1,4-戊二烯-3-酮肟酯类化合物的合成及其抑菌活性研究 总被引:1,自引:0,他引:1
以1,5-二苯基-1,4-戊二烯-3-酮肟和酰氯为原料, 合成了15个新型的1,5-二苯基-1,4-戊二烯-3-酮肟酯类化合物, 通过元素分析, IR, 1H NMR, 13C NMR等对其结构进行了表征. 初步生物活性试验结果表明, 在50 mg•L-1浓度下, 化合物3i和3o对小麦赤霉病菌抑制率分别为51.1%和 53.4%, 与对照药剂恶霉灵抑制活性相当. 相似文献
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Pinacol coupling of aromatic aldehydes by aqueous vanadium(II) solution under ultrasound irradiation at room temperature can lead to the corresponding pinacols in 54–93% yields within 15–30 min. 相似文献
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Abstract A simple, efficient, and ecofriendly procedure was developed for the synthesis of 2-substituted 1,4,5,6-tetrahydropyrimidine derivatives catalyzed by N-bromosuccinimide using ultrasonic irradiation in aqueous medium. Prominent advantages of this new method are good yields, aqueous medium, short reaction times, and easy workup procedure. The compounds were characterized by infrared, NMR, liquid chromatography–mass spectrometry, and elemental analyses. 相似文献
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Synthesis and antiviral activities of novel 1,4-pentadien-3-one derivatives bearing an emodin moiety
Jian Wu Yun-Ying Zhu Yong-Hui Zhao Wei-Li Shan De-Yu Hu Ji-Xiang Chen Deng-Yue Liu Xiang-Yang Li Song Yang 《中国化学快报》2016,27(6):948-952
A series of 1,5-diaryl-1,4-pentadien-3-one derivatives bearing an emodin group were designed and synthesized by the combination of natural products. The antiviral activities against tobacco mosaic virus (TMV) and cucumber mosaic virus (CMV) in vivo were evaluated. Some of the derivatives displayed promising curative effect and protective activity against TMV. Compound D5 showed appreciable curative bioactivity on TMV approximately of 50% at 306.2 mg/mL, which was superior to ningnanmycin (409.3 mg/mL). 相似文献
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1INTRODUCTION Antipyrine(2,3-dimethyl-1-phenyl-5-pyrazolone)and its derivatives exhibit a wide range of biological activities and applications[1~3].Antipyrine shows mi-nimal protein binding and is rapidly and completely absorbed from the gastrointestinal tract and exten-sively metabolized by the cytochrome P450liver en-zymes[4].Estimates of half-life and systemic cleara-nce of antipyrine have been used for the in vivo asse-ssment of hepatic drug oxidation in different spe-cies[5].Owing to… 相似文献
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The allylation reactions of aromatic aldehydes with allyl bromide were carried out in 89–98% yield with Sb-H2O-KF-CH3OH under ultrasound irradiation at rt for 2.5 h. The reactions in the same system gave allylic alcohols in 30–69% yield with stirring for 24 h. The main advantages of the present procedure are shorter reaction time, better yield, and environmental friendliness. 相似文献
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A series of 2-amino-6-(2-oxo-2H-chromen-3-yl)-4-pyridine-3-carbo-nitriles were synthesized by the one-pot, multicomponent reaction of 3-acetyl-coumarin, aromatic aldehydes, malononitrile, and ammonium acetate in acetic acid under microwave irradiation. The reactions were completed in 10–13 min with 61–86% yields, were environmental benign, and had easy workup. Their structures were confirmed by 1H NMR, IR, and MS spectra and elemental analysis. 相似文献
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Hlio M. T. Albuquerque Diana C. G. A. Pinto Artur M. S. Silva 《Molecules (Basel, Switzerland)》2021,26(20)
Microwave irradiation has become a popular heating technique in organic synthesis, mainly due to its short reaction times, solventless reactions, and, sometimes, higher yields. Additionally, microwave irradiation lowers energy consumption and, consequently, is ideal for optimization processes. Moreover, there is evidence that microwave irradiation can improve the regioselectivity and stereoselectivity aspects of vital importance in synthesizing bioactive compounds. These crucial features of microwave irradiation contribute to its inclusion in green chemistry procedures. Since 2003, the use of microwave-assisted organic synthesis has become common in our laboratory, making our group one of the first Portuguese research groups to implement this heating source in organic synthesis. Our achievements in the transformation of heterocyclic compounds, such as (E/Z)-3-styryl-4H-chromen-4-ones, (E)-3-(2-hydroxyphenyl)-4-styryl-1H-pyrazole, (E)-2-(4-arylbut-1-en-3-yn-1-yl)-4H-chromen-4-ones, or (E)-2-[2-(5-aryl-2-methyl-2H-1,2,3-triazol-4-yl)vinyl]-4H-chromen-4-ones, will be discussed in this review, highlighting the benefits of microwave irradiation use in organic synthesis. 相似文献
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Two different kinds of configurations of 1,4-bis[2-(4-pyridyl)ethenyl]-benzene(trans-bpeb and cis-bpeb) were achieved, and a bpeb dimer was synthesized in dimethyl sulfoxide(DMSO). Compared with the previous work that synthesized the bpeb dimer or polymer in crystal with a template agent needed, the reaction occurred in a solution phase in the present method. A hand-held ultraviolet lamp(365 nm) with the power of 12 W and the Watt density of 0.35 mW/cm2 can realize the photodimerization of bpeb, instead of the high-power mercury lamp in most previous studies. Unlike other 2+2 cycloaddition in liquid state using catalysts even noble metals, no catalysts were required here, which is cost-saving. Only the trans-pbeb can start the cycloaddition and the formation of the close J-aggregations of trans-pbeb in DMSO is a precondition for explaining the 2+2 photodimerization. The productivity for the 2+2 cycloaddition product was achieved as 55.6%. 相似文献