Beilstein J. Org. Chem.2020,16, 233–247, doi:10.3762/bjoc.16.25
Man-Man Wang Hao Huang Lei Shu Jian-Min Liu Jian-Qiu Zhang Yi-Le Yan Da-Yong Zhang School of Science, China Pharmaceutical University, Nanjing 211198, P. R. China 10.3762/bjoc.16.25 Abstract A series of aryloxyaceticacid derivatives were designed and synthesized as 4-hydoxyphenylpyruvate
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Keywords: aryloxyaceticacid; herbicidal activity; 4-hydroxyphenylpyruvate dioxygenase; modification; synthesis; Introduction
4-Hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27, HPPD), which belongs to the family of non-heme FeII-containing enzymes, is a vital enzyme for tyrosine catabolism. This enzyme
2,4-D and the 1,3-dicarbonyl unit, we designed and synthesized a series of novel aryloxyaceticacid derivatives. In this context, these derivatives were subjected to HPPD inhibition, herbicidal activity, crop safety and structure–activity relationship (SAR) studies. As expected, many of the title
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Graphical Abstract
Scheme 1:
The commonly recognized HPPD catalytic reaction mechanism.