Synthesis and Biological Activity of N-Aroyl (Aryloxyacetyl)-N′-ferrocenyl Thiourea Derivatives
Qiong Zhang
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorBihong Zhao
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorYangyang Song
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorChengwen Hua
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorXiaofeng Gou
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorBang Chen
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorCorresponding Author
Junlong Zhao
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Correspondence to: Junlong Zhao; e-mail: [email protected].Search for more papers by this authorQiong Zhang
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorBihong Zhao
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorYangyang Song
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorChengwen Hua
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorXiaofeng Gou
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorBang Chen
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Search for more papers by this authorCorresponding Author
Junlong Zhao
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069 People's Republic of China
Correspondence to: Junlong Zhao; e-mail: [email protected].Search for more papers by this authorABSTRACT
In this study, the synthesis of aminoferrocene was improved and a series of novel ferrocene-containing thiourea compounds were designed and synthesized as potential plant growth regulators. All the new compounds were characterized by IR, 1H NMR, and X-ray crystallography. Furthermore, the cytokinin and auxin activities of 5c and 5a–i were investigated. Notably, compounds 5e, 5g, and 5j in a concentration of 50 μg/mL exhibited significant cytokinin activity, and compounds 5b and 5h in a concentration of 50 μg/mL exhibited higher auxin activity than indoleacetic acid .
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