Toluene as a novel carrier of xanthates—preparation, use and surrogate of S-tri- and di-chloromethyl xanthates

Toluene has been identified as a novel carrier of xanthates. Their corresponding fragmentative precursors proved to behave efficiently in radical group transfer reactions. As examples, unprecedented S-tri/di-chloromethyl xanthates could be prepared, isolated and further used in radical additions to...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Tetrahedron letters 2014-07, Vol.55 (31), p.4410-4414
Hauptverfasser: Dumeunier, Raphaël, Huber, Annika
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4414
container_issue 31
container_start_page 4410
container_title Tetrahedron letters
container_volume 55
creator Dumeunier, Raphaël
Huber, Annika
description Toluene has been identified as a novel carrier of xanthates. Their corresponding fragmentative precursors proved to behave efficiently in radical group transfer reactions. As examples, unprecedented S-tri/di-chloromethyl xanthates could be prepared, isolated and further used in radical additions to olefins. Their precursors (de-aromatized toluene upon which is grafted, at one end, a tri/di-chloromethyl-group and, at the other end, a dithiocarbonyl group) can also be used directly in the transfer of both groups to olefins. The re-aromatizing loss of toluene by radical initiated fragmentation of the precursors brings thus new opportunities to the chemistry of xanthates, exemplified here in the intermolecular additions to olefins of new S-tri/di-chloromethyl xanthates.
doi_str_mv 10.1016/j.tetlet.2014.06.030
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1744684011</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0040403914010090</els_id><sourcerecordid>1744684011</sourcerecordid><originalsourceid>FETCH-LOGICAL-c409t-c53095245aa2f2cd4787da022e0fe2bd30f75a586f8ed062933bdbe581f3930f3</originalsourceid><addsrcrecordid>eNp9kM1KAzEUhYMoWKtv4GKWLpzxZpL52whS_IOCC3Ud0uSOTZlOxiRTdOdD-IQ-iakV3Hk3F-4958D5CDmlkFGg5cUqCxg6DFkOlGdQZsBgj0xoXbGUFTXdJxMADikH1hySI-9XEKesYUKGJ9uN2GMifSKT3m6wS5R0zqBLbJu8yT4sZUD_9fE5OBykk8HY_jwZfbT0OvGjc_YlKrbqxzQ4k_7ctUnVsrPOrjEs37u_oGNy0MrO48nvnpLnm-un2V06f7i9n13NU8WhCakqGDRFzgsp8zZXmld1pSXkOUKL-UIzaKtCFnXZ1qihzBvGFnqBsWzLmvhkU3K2yx2cfR3RB7E2XmHXyR7t6AWtOC9rDpRGKd9JlbPeO2zF4MxaundBQWwBi5XYARZbwAJKEQFH2-XOhrHGJgITXhnsFWrjUAWhrfk_4Btt-4h4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1744684011</pqid></control><display><type>article</type><title>Toluene as a novel carrier of xanthates—preparation, use and surrogate of S-tri- and di-chloromethyl xanthates</title><source>Elsevier ScienceDirect Journals Complete - AutoHoldings</source><creator>Dumeunier, Raphaël ; Huber, Annika</creator><creatorcontrib>Dumeunier, Raphaël ; Huber, Annika</creatorcontrib><description>Toluene has been identified as a novel carrier of xanthates. Their corresponding fragmentative precursors proved to behave efficiently in radical group transfer reactions. As examples, unprecedented S-tri/di-chloromethyl xanthates could be prepared, isolated and further used in radical additions to olefins. Their precursors (de-aromatized toluene upon which is grafted, at one end, a tri/di-chloromethyl-group and, at the other end, a dithiocarbonyl group) can also be used directly in the transfer of both groups to olefins. The re-aromatizing loss of toluene by radical initiated fragmentation of the precursors brings thus new opportunities to the chemistry of xanthates, exemplified here in the intermolecular additions to olefins of new S-tri/di-chloromethyl xanthates.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/j.tetlet.2014.06.030</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Carriers ; Fragmentation ; Grafting ; Olefins ; Precursors ; Radical chain ; Radicals ; Rearomatization ; Tetrahedrons ; Toluene ; Transfer reaction ; Xanthate</subject><ispartof>Tetrahedron letters, 2014-07, Vol.55 (31), p.4410-4414</ispartof><rights>2014 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-c53095245aa2f2cd4787da022e0fe2bd30f75a586f8ed062933bdbe581f3930f3</citedby><cites>FETCH-LOGICAL-c409t-c53095245aa2f2cd4787da022e0fe2bd30f75a586f8ed062933bdbe581f3930f3</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.2014.06.030$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids></links><search><creatorcontrib>Dumeunier, Raphaël</creatorcontrib><creatorcontrib>Huber, Annika</creatorcontrib><title>Toluene as a novel carrier of xanthates—preparation, use and surrogate of S-tri- and di-chloromethyl xanthates</title><title>Tetrahedron letters</title><description>Toluene has been identified as a novel carrier of xanthates. Their corresponding fragmentative precursors proved to behave efficiently in radical group transfer reactions. As examples, unprecedented S-tri/di-chloromethyl xanthates could be prepared, isolated and further used in radical additions to olefins. Their precursors (de-aromatized toluene upon which is grafted, at one end, a tri/di-chloromethyl-group and, at the other end, a dithiocarbonyl group) can also be used directly in the transfer of both groups to olefins. The re-aromatizing loss of toluene by radical initiated fragmentation of the precursors brings thus new opportunities to the chemistry of xanthates, exemplified here in the intermolecular additions to olefins of new S-tri/di-chloromethyl xanthates.</description><subject>Carriers</subject><subject>Fragmentation</subject><subject>Grafting</subject><subject>Olefins</subject><subject>Precursors</subject><subject>Radical chain</subject><subject>Radicals</subject><subject>Rearomatization</subject><subject>Tetrahedrons</subject><subject>Toluene</subject><subject>Transfer reaction</subject><subject>Xanthate</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KAzEUhYMoWKtv4GKWLpzxZpL52whS_IOCC3Ud0uSOTZlOxiRTdOdD-IQ-iakV3Hk3F-4958D5CDmlkFGg5cUqCxg6DFkOlGdQZsBgj0xoXbGUFTXdJxMADikH1hySI-9XEKesYUKGJ9uN2GMifSKT3m6wS5R0zqBLbJu8yT4sZUD_9fE5OBykk8HY_jwZfbT0OvGjc_YlKrbqxzQ4k_7ctUnVsrPOrjEs37u_oGNy0MrO48nvnpLnm-un2V06f7i9n13NU8WhCakqGDRFzgsp8zZXmld1pSXkOUKL-UIzaKtCFnXZ1qihzBvGFnqBsWzLmvhkU3K2yx2cfR3RB7E2XmHXyR7t6AWtOC9rDpRGKd9JlbPeO2zF4MxaundBQWwBi5XYARZbwAJKEQFH2-XOhrHGJgITXhnsFWrjUAWhrfk_4Btt-4h4</recordid><startdate>20140730</startdate><enddate>20140730</enddate><creator>Dumeunier, Raphaël</creator><creator>Huber, Annika</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20140730</creationdate><title>Toluene as a novel carrier of xanthates—preparation, use and surrogate of S-tri- and di-chloromethyl xanthates</title><author>Dumeunier, Raphaël ; Huber, Annika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-c53095245aa2f2cd4787da022e0fe2bd30f75a586f8ed062933bdbe581f3930f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Carriers</topic><topic>Fragmentation</topic><topic>Grafting</topic><topic>Olefins</topic><topic>Precursors</topic><topic>Radical chain</topic><topic>Radicals</topic><topic>Rearomatization</topic><topic>Tetrahedrons</topic><topic>Toluene</topic><topic>Transfer reaction</topic><topic>Xanthate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dumeunier, Raphaël</creatorcontrib><creatorcontrib>Huber, Annika</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dumeunier, Raphaël</au><au>Huber, Annika</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toluene as a novel carrier of xanthates—preparation, use and surrogate of S-tri- and di-chloromethyl xanthates</atitle><jtitle>Tetrahedron letters</jtitle><date>2014-07-30</date><risdate>2014</risdate><volume>55</volume><issue>31</issue><spage>4410</spage><epage>4414</epage><pages>4410-4414</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>Toluene has been identified as a novel carrier of xanthates. Their corresponding fragmentative precursors proved to behave efficiently in radical group transfer reactions. As examples, unprecedented S-tri/di-chloromethyl xanthates could be prepared, isolated and further used in radical additions to olefins. Their precursors (de-aromatized toluene upon which is grafted, at one end, a tri/di-chloromethyl-group and, at the other end, a dithiocarbonyl group) can also be used directly in the transfer of both groups to olefins. The re-aromatizing loss of toluene by radical initiated fragmentation of the precursors brings thus new opportunities to the chemistry of xanthates, exemplified here in the intermolecular additions to olefins of new S-tri/di-chloromethyl xanthates.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.tetlet.2014.06.030</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0040-4039
ispartof Tetrahedron letters, 2014-07, Vol.55 (31), p.4410-4414
issn 0040-4039
1873-3581
language eng
recordid cdi_proquest_miscellaneous_1744684011
source Elsevier ScienceDirect Journals Complete - AutoHoldings
subjects Carriers
Fragmentation
Grafting
Olefins
Precursors
Radical chain
Radicals
Rearomatization
Tetrahedrons
Toluene
Transfer reaction
Xanthate
title Toluene as a novel carrier of xanthates—preparation, use and surrogate of S-tri- and di-chloromethyl xanthates
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T12%3A09%3A56IST&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=Toluene%20as%20a%20novel%20carrier%20of%20xanthates%E2%80%94preparation,%20use%20and%20surrogate%20of%20S-tri-%20and%20di-chloromethyl%20xanthates&rft.jtitle=Tetrahedron%20letters&rft.au=Dumeunier,%20Rapha%C3%ABl&rft.date=2014-07-30&rft.volume=55&rft.issue=31&rft.spage=4410&rft.epage=4414&rft.pages=4410-4414&rft.issn=0040-4039&rft.eissn=1873-3581&rft_id=info:doi/10.1016/j.tetlet.2014.06.030&rft_dat=%3Cproquest_cross%3E1744684011%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=1744684011&rft_id=info:pmid/&rft_els_id=S0040403914010090&rfr_iscdi=true