Semisynthesis and acaricidal activities of isoxazole and pyrazole derivatives of a natural product bisdemethoxycurcumin

• Luo Jinxiang

  College of Plant Protection, Southwest University

• Ding Wei

  College of Plant Protection, Southwest University

• Zhang Yongqiang

  College of Plant Protection, Southwest University

• Yang Zhenguo

  College of Plant Protection, Southwest University

• Li Yang

  College of Plant Protection, Southwest University

• Ding Lijuan

  College of Plant Protection, Southwest University

Bibliographic Information

Other Title

• 天然物ビスデメトキシクルクミンのイソキサゾールおよびピラゾール誘導体の合成と殺ダニ活性

Abstract

Sixteen isoxazole and pyrazole derivatives of bisdemethoxycurcumin (BDMC) modified in β-diketone were synthesized, and their structures were confirmed by IR, ¹H NMR, ¹³C NMR, MS and elemental analysis. Preliminary acaricidal activities against female adults of Tetranychus cinnabarinus (Boisduval) and Panonychus citri (McGregor) were evaluated using the slide-dip method. The results indicated that some of these compounds exhibit more pronounced acaricidal activity than BDMC, especially compound 4, which displays acaricidal activity comparable to that of pyridaben.

Journal

• Journal of Pesticide Science

  Journal of Pesticide Science 38 (4), 214-219, 2013

  Pesticide Science Society of Japan

Keywords

• bisdemethoxycurcumin
• semisynthesis
• isoxazole
• pyrazole
• acaricidal activity

Details

• CRID: 1390282680188291328
• NII Article ID: 130004939730
• NII Book ID: AA11818622
• DOI: 10.1584/jpestics.d13-027
• COI: 1:CAS:528:DC%2BC2cXhtVOis7Y%3D
• ISSN: 13490923
• ISSN: 03851559
• ISSN: 1348589X
• NDL BIB ID: 025033869
• Web Site: http://id.ndl.go.jp/bib/025033869
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I025033869
• Web Site: https://www.jstage.jst.go.jp/article/jpestics/38/4/38_D13-027/_pdf
• Text Lang: en
• Data Source:
  • JaLC
  • NDL
  • Crossref
  • CiNii Articles
• Abstract License Flag: Disallowed