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第 34 卷第 2 期Vol. 34 No. 2
2004 年 4 月Apr 2004

所屬欄目:其它

3-芳胺甲烯基-6-甲基-6-胡椒基-5,6-二氫-2H-吡喃-2,4二酮的合成及殺菌活性
邱克明; 王有名; 何可(湖南省張家界市環(huán)保局; 元素有機化學(xué)重點(diǎn)實(shí)驗室南開(kāi)大學(xué)元素有機化學(xué)研究所; 湖南張家界)
摘 要:采用乙酰乙酸乙酯的雙負離子與胡椒基甲基酮反應,合成了5,6 二氫 6 甲基 6 胡椒基 2H 吡喃 2,4 二酮,然后與原甲酸三乙酯、芳胺進(jìn)行縮合反應,得到了3 芳胺甲烯基 5,6 二氫 6 甲基 6 胡椒基 2H 吡喃 2,4 二酮,其結構經(jīng)1HNMR和元素分析證實(shí)。生物活性初步測定表明,該類(lèi)化合物具有一定的殺菌活性。
關(guān)鍵詞:雙負離子; 胡椒基甲基酮; 殺菌
中圖分類(lèi)號:TQ455  文獻標識碼:A  文章編號:1009-9212(2004)02-0011-03
Synthesis and Fungicidal Activity of 3-Anilinomethylene-5,6-dihydro-6-methyl-6-piperonyl-2H-pyran-2, 4-diones
QIU Ke-ming~1; WANG You-ming~2; HE Ke~2 (1; Bureau of Enviroment Protection; Zhangjiajie 427000 china; 2; State Key Laboratory of Elemental-Organic Chemistry; Institute of Elemental-Organic Chemistry; Nankai University; Tianjin; 300071; China)
Abstract:5, 6-Dihydro-6-methyl-6-piperonyl-2H-pyran-2, 4-dione, which was obtained by reacting dianion of acetoacetate with piperonyl methyl acetone, reacted with substituted anilines in the presence of ethyl orthoformate and 3-anilinomethylene-5, 6-dihydro-6-methyl-6-piperonyl-2H-pyran-2, 4-diones (2) were obtained.The Structures of compounds 2 were confirmed by 1~H NMR spectra and elemental analyses. Compound 2 was tested in vitro against many fungi such as P. Zeae, A. Solani, R. Solani, P. Piricola, C. Arachidica...
Key words:Dianion; Piperonyl methyl acetone; Fungicidal activity
基金項目:國家自然科學(xué)基金青年基金資助(20302003)。
收稿日期:2004-02-17
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