Structure-Activity Relationships of Vinyl Triazole Fungicides
Four types of vinyl triazole derivatives, (Z)- and (E)-4, 4-dimethyl-l-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ones, (Z)- and (E)-4, 4-dimethyl-1-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ols have been prepared and their fungicidal activities were determined. The alcohol analogs showed high prot...
Gespeichert in:
Veröffentlicht in: | Journal of Pesticide Science 1984/05/20, Vol.9(2), pp.229-236 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 236 |
---|---|
container_issue | 2 |
container_start_page | 229 |
container_title | Journal of Pesticide Science |
container_volume | 9 |
creator | FUNAKI, Yuji ISHIGURI, Yukio KATO, Toshiro TANAKA, Shizuya |
description | Four types of vinyl triazole derivatives, (Z)- and (E)-4, 4-dimethyl-l-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ones, (Z)- and (E)-4, 4-dimethyl-1-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ols have been prepared and their fungicidal activities were determined. The alcohol analogs showed high protective activities against powdery mildew on barley (Erysiphe graminis), and brown rust on wheat (Puccinia recondita) in pot tests. Both of the ketone analogs with Z and E geometrical configurations were less active, but both of the alcohol analogs showed high activities. The activities of the E-alcohol analogs against both diseases were the highest. The E-alcohol analogs also showed excellent systemic activities and broad fungitoxic spectra. Such halogen substituents on the phenyl ring as 4-Cl, 2, 4-Cl2 and 2-F, 4-Cl of the E-alchohol analogs were favorable to the higher protective activities. |
doi_str_mv | 10.1584/jpestics.9.229 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1444150346</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3106663631</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-b44be11df5b586f7ac163c7d2eb97ee5a313593b93fa8fe9733428032ca796243</originalsourceid><addsrcrecordid>eNo9kNFLwzAQh4MoOOZefS743Jr0krZ58GEMp8JA0Cm-hTS7bhm1rUkqzL_ebtM9HHcP33fH_Qi5ZjRhouC32w59sMYnMklTeUZGDLiMqUzh_DAXsSjkxyWZeG9LSoExwaUYkbvX4HoTeofx1AT7bcMuesFaB9s2fmM7H7VV9G6bXR0tndU_bY3RvG_W1tgV-ityUena4-Svj8nb_H45e4wXzw9Ps-kiNpDTEJecl8jYqhKlKLIq14ZlYPJViqXMEYUGBkJCKaHSRYUyB-BpQSE1OpdZymFMbo57O9d-9cOnatv2rhlOKsY5Z4ICzwYqOVLGtd47rFTn7Kd2O8Wo2qek_lNSUg0pDcL8KGx90Gs84doNUI0nnMlc7JVDDeIJMBvtFDbwC9h1dlg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1444150346</pqid></control><display><type>article</type><title>Structure-Activity Relationships of Vinyl Triazole Fungicides</title><source>J-STAGE Free</source><creator>FUNAKI, Yuji ; ISHIGURI, Yukio ; KATO, Toshiro ; TANAKA, Shizuya</creator><creatorcontrib>FUNAKI, Yuji ; ISHIGURI, Yukio ; KATO, Toshiro ; TANAKA, Shizuya</creatorcontrib><description>Four types of vinyl triazole derivatives, (Z)- and (E)-4, 4-dimethyl-l-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ones, (Z)- and (E)-4, 4-dimethyl-1-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ols have been prepared and their fungicidal activities were determined. The alcohol analogs showed high protective activities against powdery mildew on barley (Erysiphe graminis), and brown rust on wheat (Puccinia recondita) in pot tests. Both of the ketone analogs with Z and E geometrical configurations were less active, but both of the alcohol analogs showed high activities. The activities of the E-alcohol analogs against both diseases were the highest. The E-alcohol analogs also showed excellent systemic activities and broad fungitoxic spectra. Such halogen substituents on the phenyl ring as 4-Cl, 2, 4-Cl2 and 2-F, 4-Cl of the E-alchohol analogs were favorable to the higher protective activities.</description><identifier>ISSN: 1348-589X</identifier><identifier>EISSN: 1349-0923</identifier><identifier>DOI: 10.1584/jpestics.9.229</identifier><language>eng</language><publisher>Tokyo: Pesticide Science Society of Japan</publisher><ispartof>Journal of Pesticide Science, 1984/05/20, Vol.9(2), pp.229-236</ispartof><rights>Pesticide Science Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 1984</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-b44be11df5b586f7ac163c7d2eb97ee5a313593b93fa8fe9733428032ca796243</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1876,27903,27904</link.rule.ids></links><search><creatorcontrib>FUNAKI, Yuji</creatorcontrib><creatorcontrib>ISHIGURI, Yukio</creatorcontrib><creatorcontrib>KATO, Toshiro</creatorcontrib><creatorcontrib>TANAKA, Shizuya</creatorcontrib><title>Structure-Activity Relationships of Vinyl Triazole Fungicides</title><title>Journal of Pesticide Science</title><addtitle>J. Pestic. Sci.</addtitle><description>Four types of vinyl triazole derivatives, (Z)- and (E)-4, 4-dimethyl-l-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ones, (Z)- and (E)-4, 4-dimethyl-1-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ols have been prepared and their fungicidal activities were determined. The alcohol analogs showed high protective activities against powdery mildew on barley (Erysiphe graminis), and brown rust on wheat (Puccinia recondita) in pot tests. Both of the ketone analogs with Z and E geometrical configurations were less active, but both of the alcohol analogs showed high activities. The activities of the E-alcohol analogs against both diseases were the highest. The E-alcohol analogs also showed excellent systemic activities and broad fungitoxic spectra. Such halogen substituents on the phenyl ring as 4-Cl, 2, 4-Cl2 and 2-F, 4-Cl of the E-alchohol analogs were favorable to the higher protective activities.</description><issn>1348-589X</issn><issn>1349-0923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNo9kNFLwzAQh4MoOOZefS743Jr0krZ58GEMp8JA0Cm-hTS7bhm1rUkqzL_ebtM9HHcP33fH_Qi5ZjRhouC32w59sMYnMklTeUZGDLiMqUzh_DAXsSjkxyWZeG9LSoExwaUYkbvX4HoTeofx1AT7bcMuesFaB9s2fmM7H7VV9G6bXR0tndU_bY3RvG_W1tgV-ityUena4-Svj8nb_H45e4wXzw9Ps-kiNpDTEJecl8jYqhKlKLIq14ZlYPJViqXMEYUGBkJCKaHSRYUyB-BpQSE1OpdZymFMbo57O9d-9cOnatv2rhlOKsY5Z4ICzwYqOVLGtd47rFTn7Kd2O8Wo2qek_lNSUg0pDcL8KGx90Gs84doNUI0nnMlc7JVDDeIJMBvtFDbwC9h1dlg</recordid><startdate>19840101</startdate><enddate>19840101</enddate><creator>FUNAKI, Yuji</creator><creator>ISHIGURI, Yukio</creator><creator>KATO, Toshiro</creator><creator>TANAKA, Shizuya</creator><general>Pesticide Science Society of Japan</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7ST</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>19840101</creationdate><title>Structure-Activity Relationships of Vinyl Triazole Fungicides</title><author>FUNAKI, Yuji ; ISHIGURI, Yukio ; KATO, Toshiro ; TANAKA, Shizuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-b44be11df5b586f7ac163c7d2eb97ee5a313593b93fa8fe9733428032ca796243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FUNAKI, Yuji</creatorcontrib><creatorcontrib>ISHIGURI, Yukio</creatorcontrib><creatorcontrib>KATO, Toshiro</creatorcontrib><creatorcontrib>TANAKA, Shizuya</creatorcontrib><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Journal of Pesticide Science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FUNAKI, Yuji</au><au>ISHIGURI, Yukio</au><au>KATO, Toshiro</au><au>TANAKA, Shizuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure-Activity Relationships of Vinyl Triazole Fungicides</atitle><jtitle>Journal of Pesticide Science</jtitle><addtitle>J. Pestic. Sci.</addtitle><date>1984-01-01</date><risdate>1984</risdate><volume>9</volume><issue>2</issue><spage>229</spage><epage>236</epage><pages>229-236</pages><issn>1348-589X</issn><eissn>1349-0923</eissn><abstract>Four types of vinyl triazole derivatives, (Z)- and (E)-4, 4-dimethyl-l-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ones, (Z)- and (E)-4, 4-dimethyl-1-phenyl-2-(1, 2, 4-triazol-1-y1)-1-penten-3-ols have been prepared and their fungicidal activities were determined. The alcohol analogs showed high protective activities against powdery mildew on barley (Erysiphe graminis), and brown rust on wheat (Puccinia recondita) in pot tests. Both of the ketone analogs with Z and E geometrical configurations were less active, but both of the alcohol analogs showed high activities. The activities of the E-alcohol analogs against both diseases were the highest. The E-alcohol analogs also showed excellent systemic activities and broad fungitoxic spectra. Such halogen substituents on the phenyl ring as 4-Cl, 2, 4-Cl2 and 2-F, 4-Cl of the E-alchohol analogs were favorable to the higher protective activities.</abstract><cop>Tokyo</cop><pub>Pesticide Science Society of Japan</pub><doi>10.1584/jpestics.9.229</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1348-589X |
ispartof | Journal of Pesticide Science, 1984/05/20, Vol.9(2), pp.229-236 |
issn | 1348-589X 1349-0923 |
language | eng |
recordid | cdi_proquest_journals_1444150346 |
source | J-STAGE Free |
title | Structure-Activity Relationships of Vinyl Triazole Fungicides |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T06%3A49%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structure-Activity%20Relationships%20of%20Vinyl%20Triazole%20Fungicides&rft.jtitle=Journal%20of%20Pesticide%20Science&rft.au=FUNAKI,%20Yuji&rft.date=1984-01-01&rft.volume=9&rft.issue=2&rft.spage=229&rft.epage=236&rft.pages=229-236&rft.issn=1348-589X&rft.eissn=1349-0923&rft_id=info:doi/10.1584/jpestics.9.229&rft_dat=%3Cproquest_cross%3E3106663631%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1444150346&rft_id=info:pmid/&rfr_iscdi=true |