-
- Ogawa Narihito
- Department of Applied Chemistry, Meiji University
-
- Imaizumi Ryoya
- Department of Applied Chemistry, Meiji University
-
- Hirano Tatsuya
- Hokko Chemical Industry Co., Ltd.
-
- Suzuki Jun
- Hokko Chemical Industry Co., Ltd.
この論文をさがす
抄録
<p>We investigated the synthesis and herbicidal activity of 23 toxoflavin analogs, 1a–w, in which aromatic rings (R) were introduced into the C-3 position. In paddy field conditions, 1k (R=2-CF3–C6H4) and 1w (R=2-thienyl) showed excellent herbicidal activity. Under upland field conditions, we found that toxoflavin analogs 1a (R=C6H5), 1n (R=2-CH3O–C6H4), and 1p (R=4-CH3O–C6H4) exhibited wide herbicidal spectrum against Echinochloa crus-galli (L) var. crus-galli (ECHCG), Chenopodium album, and Amaranthus viridis (AMAVI). The analog with the 2-fluoro group on benzene ring 1b also showed high herbicidal activity against both ECHCG and AMAVI.</p>
収録刊行物
-
- 日本農薬学会誌(Journal of Pesticide Science)
-
日本農薬学会誌(Journal of Pesticide Science) 46 (3), 278-282, 2021-08-20
日本農薬学会
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1390852174975895168
-
- NII論文ID
- 130008080971
-
- NII書誌ID
- AA11818622
-
- ISSN
- 13490923
- 03851559
- 1348589X
-
- NDL書誌ID
- 031829987
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- NDL
- Crossref
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可