Synthesis and Fungicidal Activities of Phenoxyphenyl Alkoxyiminoacetamide Derivatives
-
- KATAOKA Takahiro
- Bulk Chemicals Manufacturing Technical Service Dept., Shionogi & Co., Ltd.
-
- HAYASE Yoshio
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- MASUKO Michio
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- NIIKAWA Motomu
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- ICHINARI Mitsuhiro
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- TAKENAKA Hideyuki
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- TANIMOTO Norihiko
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- HAYASHI Yoshiyuki
- Aburahi Laboratories, Shionogi & Co., Ltd.
-
- TAKEDA Reiji
- Technology Coordination Dept., Shionogi & Co., Ltd.
Bibliographic Information
- Other Title
-
- フェノキシフェニルアルコキシイミノアセトアミド誘導体の合成と殺菌活性
- Synthesis and Fungicidal Activities of
- Structure and Fungicidal Activities of New Alkoxyiminoacetamide Derivatives (Part 1)
Search this article
Abstract
A number of alkoxyiminophenylacetamide derivatives were synthesized and their fungicidal activities were examined. Studies of structure-activity relationships revealed strongest fungicidal activity when the alkoxyimino moiety and the acetamide moiety were each substituted with a methyl group. When the 2-position of the benzene ring on the phenylacetamide moiety was substituted with a phenoxy or phenoxymethyl group, good fungicidal activity was obtained. Introduction of other substituents on the benzene ring of the phenylacetamide moiety resulted in decrease of the fungicidal activity. However, introduction of some substituents on the benzene ring of the 2-phenoxy group increased the activity to some extent. Between the two oxime geometrical isomers, the activity of the E-form was much stronger than that of the Z-form. Consequently, (E)-2-methoxyimino-N-methyl-2-(2-phenoxyphenyl)acetamide was selected as a candidate fungicide for rice diseases.
Journal
-
- Journal of Pesticide Science
-
Journal of Pesticide Science 23 (2), 95-106, 1998
Pesticide Science Society of Japan
- Tweet
Details 詳細情報について
-
- CRID
- 1390282680186603392
-
- NII Article ID
- 110001713032
-
- NII Book ID
- AN00196227
-
- ISSN
- 03851559
- 13490923
- 1348589X
-
- NDL BIB ID
- 4502844
-
- Data Source
-
- JaLC
- IRDB
- NDL
- Crossref
- NDL-Digital
- CiNii Articles
-
- Abstract License Flag
- Disallowed