On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers

On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers

Two two-compound mixtures of candidate structures for the Phytophthora α1 mating hormone have been synthesized. The mixtures were designed to have differing configurations at C3, but proved to be identical. This suggests that epimerization occurred at C3, and comparison with the data for the natural...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Tetrahedron letters 2007-11, Vol.48 (45), p.7965-7968
Hauptverfasser: Bajpai, Reena, Yang, Fanglong, Curran, Dennis P.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 7968
container_issue 45
container_start_page 7965
container_title Tetrahedron letters
container_volume 48
creator Bajpai, Reena
Yang, Fanglong
Curran, Dennis P.
description Two two-compound mixtures of candidate structures for the Phytophthora α1 mating hormone have been synthesized. The mixtures were designed to have differing configurations at C3, but proved to be identical. This suggests that epimerization occurred at C3, and comparison with the data for the natural samples suggest that this is also a mixture of isomers.
doi_str_mv 10.1016/j.tetlet.2007.09.054
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2083561</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0040403907018229</els_id><sourcerecordid>1835548396</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4444-9d2cea91d81a6136d0f2c202c0d27c5b6a50dbb823976400a18614b5224279d3</originalsourceid><addsrcrecordid>eNp9kc2OFCEQx4nRuOPqGxjD0Uu3Bf0FHkzMxq9kk_Wwd0JD9Q6TbpgFepN5LF_EZ5JxJq5erAuh6l-_gvoT8ppBzYD173Z1xjxjrjnAUIOsoWufkA0TQ1M1nWBPyQaghaqFRl6QFyntoEQv4Dm5YEIK2XT9htzfeJq3SFOOq8lrRBqm34nv20MO-23ehqjpzx-MLjo7f0fLfQke39N08EWXXKLaW2rCstfRpeCPgCmskZqSd1bnIxwjhlJcMKaX5Nmk54Svzucluf386fbqa3V98-Xb1cfryrQlKmm5QS2ZFUz3rOktTNxw4AYsH0w39roDO46CN3LoWwDNRM_aseO85YO0zSX5cMLu13FBa9DnqGe1j27R8aCCdurfindbdRceFAdRNsMK4O0ZEMP9iimrxSWD86w9hjUpVmRdKxrZF2l7kpoYUoo4_RnDQB3NUjt1MksdzVIgVTGrtL35-4mPTWd3Hv-AZU8PDqNKxqE3aF1Ek5UN7v8TfgFwUasm</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1835548396</pqid></control><display><type>article</type><title>On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Bajpai, Reena ; Yang, Fanglong ; Curran, Dennis P.</creator><creatorcontrib>Bajpai, Reena ; Yang, Fanglong ; Curran, Dennis P.</creatorcontrib><description>Two two-compound mixtures of candidate structures for the Phytophthora α1 mating hormone have been synthesized. The mixtures were designed to have differing configurations at C3, but proved to be identical. This suggests that epimerization occurred at C3, and comparison with the data for the natural samples suggest that this is also a mixture of isomers.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/j.tetlet.2007.09.054</identifier><identifier>PMID: 18989356</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><ispartof>Tetrahedron letters, 2007-11, Vol.48 (45), p.7965-7968</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4444-9d2cea91d81a6136d0f2c202c0d27c5b6a50dbb823976400a18614b5224279d3</citedby><cites>FETCH-LOGICAL-c4444-9d2cea91d81a6136d0f2c202c0d27c5b6a50dbb823976400a18614b5224279d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tetlet.2007.09.054$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18989356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bajpai, Reena</creatorcontrib><creatorcontrib>Yang, Fanglong</creatorcontrib><creatorcontrib>Curran, Dennis P.</creatorcontrib><title>On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers</title><title>Tetrahedron letters</title><addtitle>Tetrahedron Lett</addtitle><description>Two two-compound mixtures of candidate structures for the Phytophthora α1 mating hormone have been synthesized. The mixtures were designed to have differing configurations at C3, but proved to be identical. This suggests that epimerization occurred at C3, and comparison with the data for the natural samples suggest that this is also a mixture of isomers.</description><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kc2OFCEQx4nRuOPqGxjD0Uu3Bf0FHkzMxq9kk_Wwd0JD9Q6TbpgFepN5LF_EZ5JxJq5erAuh6l-_gvoT8ppBzYD173Z1xjxjrjnAUIOsoWufkA0TQ1M1nWBPyQaghaqFRl6QFyntoEQv4Dm5YEIK2XT9htzfeJq3SFOOq8lrRBqm34nv20MO-23ehqjpzx-MLjo7f0fLfQke39N08EWXXKLaW2rCstfRpeCPgCmskZqSd1bnIxwjhlJcMKaX5Nmk54Svzucluf386fbqa3V98-Xb1cfryrQlKmm5QS2ZFUz3rOktTNxw4AYsH0w39roDO46CN3LoWwDNRM_aseO85YO0zSX5cMLu13FBa9DnqGe1j27R8aCCdurfindbdRceFAdRNsMK4O0ZEMP9iimrxSWD86w9hjUpVmRdKxrZF2l7kpoYUoo4_RnDQB3NUjt1MksdzVIgVTGrtL35-4mPTWd3Hv-AZU8PDqNKxqE3aF1Ek5UN7v8TfgFwUasm</recordid><startdate>20071105</startdate><enddate>20071105</enddate><creator>Bajpai, Reena</creator><creator>Yang, Fanglong</creator><creator>Curran, Dennis P.</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20071105</creationdate><title>On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers</title><author>Bajpai, Reena ; Yang, Fanglong ; Curran, Dennis P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4444-9d2cea91d81a6136d0f2c202c0d27c5b6a50dbb823976400a18614b5224279d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bajpai, Reena</creatorcontrib><creatorcontrib>Yang, Fanglong</creatorcontrib><creatorcontrib>Curran, Dennis P.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bajpai, Reena</au><au>Yang, Fanglong</au><au>Curran, Dennis P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers</atitle><jtitle>Tetrahedron letters</jtitle><addtitle>Tetrahedron Lett</addtitle><date>2007-11-05</date><risdate>2007</risdate><volume>48</volume><issue>45</issue><spage>7965</spage><epage>7968</epage><pages>7965-7968</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>Two two-compound mixtures of candidate structures for the Phytophthora α1 mating hormone have been synthesized. The mixtures were designed to have differing configurations at C3, but proved to be identical. This suggests that epimerization occurred at C3, and comparison with the data for the natural samples suggest that this is also a mixture of isomers.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>18989356</pmid><doi>10.1016/j.tetlet.2007.09.054</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0040-4039
ispartof Tetrahedron letters, 2007-11, Vol.48 (45), p.7965-7968
issn 0040-4039
1873-3581
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2083561
source Elsevier ScienceDirect Journals Complete
title On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T01%3A25%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=On%20the%20structure%20of%20the%20Phytophthora%20%CE%B11%20mating%20hormone:%20synthesis%20and%20comparison%20of%20four%20candidate%20stereoisomers&rft.jtitle=Tetrahedron%20letters&rft.au=Bajpai,%20Reena&rft.date=2007-11-05&rft.volume=48&rft.issue=45&rft.spage=7965&rft.epage=7968&rft.pages=7965-7968&rft.issn=0040-4039&rft.eissn=1873-3581&rft_id=info:doi/10.1016/j.tetlet.2007.09.054&rft_dat=%3Cproquest_pubme%3E1835548396%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1835548396&rft_id=info:pmid/18989356&rft_els_id=S0040403907018229&rfr_iscdi=true