The pyrethrins and related compounds. Part XXXV. Esters of aryl-substituted cyclopentane alcohols and analogues
Synthesis of a range of 1‐, 2‐and 3‐phenyl, benzyl and phenethyl substituted cyclopentanols and cyclopentylmethyl alcohols and related unsaturated compounds is reported. Results of bioassays of their esters with known pyrethroidal acids against two species of insect lead to recognition of some struc...
Gespeichert in:
| Veröffentlicht in: | Pesticide Science 1989, Vol.25 (2), p.205-218 |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 218 |
|---|---|
| container_issue | 2 |
| container_start_page | 205 |
| container_title | Pesticide Science |
| container_volume | 25 |
| creator | Farnham, Andrew W. Janes, Norman F. Khambay, Bhupinder P. S. |
| description | Synthesis of a range of 1‐, 2‐and 3‐phenyl, benzyl and phenethyl substituted cyclopentanols and cyclopentylmethyl alcohols and related unsaturated compounds is reported. Results of bioassays of their esters with known pyrethroidal acids against two species of insect lead to recognition of some structure‐activity relationships in this series. The distance and relative orientation between the alcoholic and aryl functions appears crucial, but in other respects the nature of the spacer group between them is less important. The most effective alcoholic components are based on cyclopentenes. |
| doi_str_mv | 10.1002/ps.2780250212 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1877108512</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1877108512</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2662-f1a0a3ec835788693565e2ec0971878ce04390edecd516a3e7fa5d1e52f529703</originalsourceid><addsrcrecordid>eNp9kDlPxDAQhS0EEstR0luizjK2sR2X3CCtOMS1nWWcCRsIcbATwf57AotANFTTfO-YR8gWgzED4DttGnOdA5fAGV8iIwZGZQaUWCYjAMEyxcR0layl9AQAxhgxIuFmhrSdR-xmsWoSdU1BI9auw4L68NKGvinSmF662NHpdHo3pkepw5hoKKmL8zpL_UPqqq7_Esx9HVpsOtcgdbUPs1AvLF3j6vDYY9ogK6WrE25-33Vye3x0c3CaTS5Ozg72JpnnSvGsZA6cQJ8LqfNcGSGVRI4ejGa5zj3CrjCABfpCMjWQunSyYCh5KbnRINbJ9sK3jeF1yO3sU-jj0CLZwUAzyCXjA5UtKB9DShFL28bqZfjLMrCfm9o22d9NB14v-Leqxvn_sL28_qP8TqqG-d5_lC4-W6WFlvb-_MTuH_LzyfWVtiA-AKxMiX4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1877108512</pqid></control><display><type>article</type><title>The pyrethrins and related compounds. Part XXXV. Esters of aryl-substituted cyclopentane alcohols and analogues</title><source>Wiley Online Library Journals Frontfile Complete</source><source>Periodicals Index Online</source><creator>Farnham, Andrew W. ; Janes, Norman F. ; Khambay, Bhupinder P. S.</creator><creatorcontrib>Farnham, Andrew W. ; Janes, Norman F. ; Khambay, Bhupinder P. S.</creatorcontrib><description>Synthesis of a range of 1‐, 2‐and 3‐phenyl, benzyl and phenethyl substituted cyclopentanols and cyclopentylmethyl alcohols and related unsaturated compounds is reported. Results of bioassays of their esters with known pyrethroidal acids against two species of insect lead to recognition of some structure‐activity relationships in this series. The distance and relative orientation between the alcoholic and aryl functions appears crucial, but in other respects the nature of the spacer group between them is less important. The most effective alcoholic components are based on cyclopentenes.</description><identifier>ISSN: 0031-613X</identifier><identifier>ISSN: 1526-498X</identifier><identifier>EISSN: 1096-9063</identifier><identifier>DOI: 10.1002/ps.2780250212</identifier><language>eng</language><publisher>London: John Wiley & Sons, Ltd</publisher><ispartof>Pesticide Science, 1989, Vol.25 (2), p.205-218</ispartof><rights>Copyright © 1989 John Wiley & Sons, Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2662-f1a0a3ec835788693565e2ec0971878ce04390edecd516a3e7fa5d1e52f529703</citedby><cites>FETCH-LOGICAL-c2662-f1a0a3ec835788693565e2ec0971878ce04390edecd516a3e7fa5d1e52f529703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fps.2780250212$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fps.2780250212$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27846,27900,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Farnham, Andrew W.</creatorcontrib><creatorcontrib>Janes, Norman F.</creatorcontrib><creatorcontrib>Khambay, Bhupinder P. S.</creatorcontrib><title>The pyrethrins and related compounds. Part XXXV. Esters of aryl-substituted cyclopentane alcohols and analogues</title><title>Pesticide Science</title><addtitle>Pestic. Sci</addtitle><description>Synthesis of a range of 1‐, 2‐and 3‐phenyl, benzyl and phenethyl substituted cyclopentanols and cyclopentylmethyl alcohols and related unsaturated compounds is reported. Results of bioassays of their esters with known pyrethroidal acids against two species of insect lead to recognition of some structure‐activity relationships in this series. The distance and relative orientation between the alcoholic and aryl functions appears crucial, but in other respects the nature of the spacer group between them is less important. The most effective alcoholic components are based on cyclopentenes.</description><issn>0031-613X</issn><issn>1526-498X</issn><issn>1096-9063</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>K30</sourceid><recordid>eNp9kDlPxDAQhS0EEstR0luizjK2sR2X3CCtOMS1nWWcCRsIcbATwf57AotANFTTfO-YR8gWgzED4DttGnOdA5fAGV8iIwZGZQaUWCYjAMEyxcR0layl9AQAxhgxIuFmhrSdR-xmsWoSdU1BI9auw4L68NKGvinSmF662NHpdHo3pkepw5hoKKmL8zpL_UPqqq7_Esx9HVpsOtcgdbUPs1AvLF3j6vDYY9ogK6WrE25-33Vye3x0c3CaTS5Ozg72JpnnSvGsZA6cQJ8LqfNcGSGVRI4ejGa5zj3CrjCABfpCMjWQunSyYCh5KbnRINbJ9sK3jeF1yO3sU-jj0CLZwUAzyCXjA5UtKB9DShFL28bqZfjLMrCfm9o22d9NB14v-Leqxvn_sL28_qP8TqqG-d5_lC4-W6WFlvb-_MTuH_LzyfWVtiA-AKxMiX4</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>Farnham, Andrew W.</creator><creator>Janes, Norman F.</creator><creator>Khambay, Bhupinder P. S.</creator><general>John Wiley & Sons, Ltd</general><general>London :John Wiley & Sons Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7WH</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope></search><sort><creationdate>1989</creationdate><title>The pyrethrins and related compounds. Part XXXV. Esters of aryl-substituted cyclopentane alcohols and analogues</title><author>Farnham, Andrew W. ; Janes, Norman F. ; Khambay, Bhupinder P. S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2662-f1a0a3ec835788693565e2ec0971878ce04390edecd516a3e7fa5d1e52f529703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Farnham, Andrew W.</creatorcontrib><creatorcontrib>Janes, Norman F.</creatorcontrib><creatorcontrib>Khambay, Bhupinder P. S.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 50</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><jtitle>Pesticide Science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farnham, Andrew W.</au><au>Janes, Norman F.</au><au>Khambay, Bhupinder P. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The pyrethrins and related compounds. Part XXXV. Esters of aryl-substituted cyclopentane alcohols and analogues</atitle><jtitle>Pesticide Science</jtitle><addtitle>Pestic. Sci</addtitle><date>1989</date><risdate>1989</risdate><volume>25</volume><issue>2</issue><spage>205</spage><epage>218</epage><pages>205-218</pages><issn>0031-613X</issn><issn>1526-498X</issn><eissn>1096-9063</eissn><abstract>Synthesis of a range of 1‐, 2‐and 3‐phenyl, benzyl and phenethyl substituted cyclopentanols and cyclopentylmethyl alcohols and related unsaturated compounds is reported. Results of bioassays of their esters with known pyrethroidal acids against two species of insect lead to recognition of some structure‐activity relationships in this series. The distance and relative orientation between the alcoholic and aryl functions appears crucial, but in other respects the nature of the spacer group between them is less important. The most effective alcoholic components are based on cyclopentenes.</abstract><cop>London</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/ps.2780250212</doi><tpages>14</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0031-613X |
| ispartof | Pesticide Science, 1989, Vol.25 (2), p.205-218 |
| issn | 0031-613X 1526-498X 1096-9063 |
| language | eng |
| recordid | cdi_proquest_journals_1877108512 |
| source | Wiley Online Library Journals Frontfile Complete; Periodicals Index Online |
| title | The pyrethrins and related compounds. Part XXXV. Esters of aryl-substituted cyclopentane alcohols and analogues |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T07%3A46%3A38IST&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=The%20pyrethrins%20and%20related%20compounds.%20Part%20XXXV.%20Esters%20of%20aryl-substituted%20cyclopentane%20alcohols%20and%20analogues&rft.jtitle=Pesticide%20Science&rft.au=Farnham,%20Andrew%20W.&rft.date=1989&rft.volume=25&rft.issue=2&rft.spage=205&rft.epage=218&rft.pages=205-218&rft.issn=0031-613X&rft.eissn=1096-9063&rft_id=info:doi/10.1002/ps.2780250212&rft_dat=%3Cproquest_cross%3E1877108512%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=1877108512&rft_id=info:pmid/&rfr_iscdi=true |