دورية أكاديمية

The Synthesis and Biological Activity of 1-Alkyl-4-(3-azacyclobenzoyl)-5-hydroxypyrazole Herbicides

التفاصيل البيبلوغرافية
العنوان: The Synthesis and Biological Activity of 1-Alkyl-4-(3-azacyclobenzoyl)-5-hydroxypyrazole Herbicides
المؤلفون: Zoltan Benko, Sharon Shinkle, John Van Heertum, Johnny Jackson, Jeffery McQuiston, Jeffery Webster, James Turner, Monte Weimer, Eileen Paterson
المصدر: CHIMIA, Vol 57, Iss 11 (2003)
بيانات النشر: Swiss Chemical Society, 2003.
سنة النشر: 2003
المجموعة: LCC:Chemistry
مصطلحات موضوعية: Benzoylpyrazoles, Herbicide, Hydroxyphenylpyruvate dioxygenase inhibitors, Morpholines, Piperidines, Chemistry, QD1-999
الوصف: The benzoylpyrazoles belong to a class of herbicides that inhibit the enzyme 4-hydroxy-phenylpyruvate dioxygenase (HPPD). This mode of action is characterized by bleaching due to the disruption of plastoquinone and ?-tocopherol biosynthesis. Early studies indicated that the C(3) position of benzoylpyrazoles can accommodate a wide range of functionality. This paper describes synthetic efforts to improve cool season grass weed activity and wheat selectivity by incorporating cyclic moieties attached through nitrogen at this position. The aza substituents were generally installed by nucleophilic aromatic substitution, however, an efficient four-step method was developed for constructing substituted morpholino moieties directly on pre-formed benzoylpyrazoles. The structure–activity relationships revealed that certain piperidino moieties provided good activity on wild oat, while exhibiting selectivity toward wheat. They also showed that excellent levels of activity on wild oat and blackgrass can be achieved with morpholino substituents.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: German
English
French
تدمد: 0009-4293
2673-2424
Relation: https://chimia.ch/chimia/article/view/3775; https://doaj.org/toc/0009-4293; https://doaj.org/toc/2673-2424
DOI: 10.2533/000942903777678579
URL الوصول: https://doaj.org/article/6de7782580fd49e29e11693296c13940
رقم الأكسشن: edsdoj.6de7782580fd49e29e11693296c13940
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:00094293
26732424
DOI:10.2533/000942903777678579