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Synthesis and anti-oomycete activity of novel quinazolin- and benzothiazol-6-yloxyacetamides: Potent aza-analogs and five-ring analogs of quinoline fungicides

机译:新型喹唑啉-和苯并噻唑-6-酰氧基乙酰胺的合成及其抗卵菌活性:有效的氮杂类似物和喹啉类杀菌剂的五环类似物

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摘要

Novel quinazolin-and benzothiazol-6-yloxyacetamides show excellent in vivo activity against the three economically most important Oomycete pathogens Phytophthora infestans, Plasmopara viticola and Pythium ultimum. They are polar analogs of known quinolin-6-yloxyacetamides, which are not active against the soil-borne damping-off disease caused by Pythium ultimum. The Bogert quinazoline synthesis, an almost forgotten heterocyclization technique, proved to be highly useful for the concise construction of required quinazolin-6-ol building blocks. (C) 2015 Elsevier Ltd. All rights reserved.
机译:新型喹唑啉-和苯并噻唑-6-酰氧基乙酰胺显示出对三种经济上最重要的卵菌病原菌疫霉菌,小生霉菌和终极腐霉菌具有优异的体内活性。它们是已知的喹啉-6-基氧基乙酰胺的极性类似物,对由终极腐霉引起的土壤传播的抑制病没有活性。 Bogert喹唑啉合成(一种几乎被遗忘的杂环化技术)被证明对于所需的quinazolin-6-ol构建基团的简洁构建非常有用。 (C)2015 Elsevier Ltd.保留所有权利。

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