Synthesis and fungicidal activity of novel imidazole-based ketene dithioacetals

被引：17

作者：

Jeanmart, Stephane ^{[1
]}

Gagnepain, Julien ^{[1
]}

Maity, Pulakesh ^{[2
]}

Lamberth, Clemens ^{[1
]}

Cederbaum, Fredrik ^{[1
]}

Rajan, Ramya ^{[2
]}

Jacob, Olivier ^{[1
]}

Blum, Mathias ^{[1
]}

Bieri, Stephane ^{[1
]}

机构：

[1] Syngenta Crop Protect AG, Chem Res, Schaffhauserstr 101, CH-4332 Stein, Switzerland

[2] Syngenta Biosci Pvt Ltd, Res & Technol Ctr, Santa Monica Works, Ilhas 403110, Goa, India

来源：

BIOORGANIC & MEDICINAL CHEMISTRY | 2018年 / 26卷 / 08期

关键词：

Dithiolane; Imidazole; C14-demethylase inhibitor; Fungicide; Crop protection; N-3-PYRIDYLDITHIOCARBONIMIDATE S-1358; ANTIFUNGAL AGENT; CYP51; DERIVATIVES; CHLOROHYDRINS; LANOCONAZOLE; LULICONAZOLE; RESISTANCE; CHEMISTRY; DENMERT;

D O I：

10.1016/j.bmc.2018.02.051

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

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 14 alpha -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. (C) 2018 Elsevier Ltd. All rights reserved.

引用

页码：2009 / 2016

页数：8

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