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新型咪唑基偕二硫代缩醛酮的合成与杀菌活性。

Synthesis and fungicidal activity of novel imidazole-based ketene dithioacetals.

机构信息

Syngenta Crop Protection AG, Chemical Research, Schaffhauserstr. 101, CH-4332 Stein, Switzerland.

Syngenta Biosciences Pvt. Ltd, Research & Technology Centre, Santa Monica Works, Corlim, Ilhas, Goa 403 110, India.

出版信息

Bioorg Med Chem. 2018 May 1;26(8):2009-2016. doi: 10.1016/j.bmc.2018.02.051. Epub 2018 Mar 9.

Abstract

Novel imidazole-based ketene dithioacetals show impressive in planta activity against the economically important plant pathogens Alternaria solani, Botryotinia fuckeliana, Erysiphe necator and Zymoseptoria tritici. Especially derivatives of the topical antifungal lanoconazole, which bear an alkynyloxy or a heteroaryl group in the para-position of the phenyl ring, exhibit excellent control of the mentioned phytopathogens. These compounds inhibit 14α -demethylase in the sterol biosynthesis pathway of the fungi. Synthesis routes starting from either benzaldehydes or acetophenones as well as structure-activity relationships are discussed in detail.

摘要

新型咪唑基偕二硫缩醛类化合物对经济上重要的植物病原体茄镰孢菌、葡萄座腔菌、苹果黑星菌和玉蜀黍平脐蠕孢菌具有显著的体内活性。特别是含有炔氧基或杂芳基取代基的局部抗真菌药物兰康唑的衍生物,对上述植物病原体表现出优异的防治效果。这些化合物抑制真菌甾醇生物合成途径中的 14α-去甲基酶。详细讨论了以苯甲醛或苯乙酮为起始原料的合成路线以及构效关系。

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