Stereoselective Synthesis of Alkenyl Silanes, Sulfones, Phosphine Oxides, and Nitroolefins by Radical C–S Bond Cleavage of Arylalkenyl Sulfides
A radical-mediated approach has been introduced for the C–S bond activation of arylalkenyl sulfides. The protocol provides an efficient approach for the generation of various alkenes including alkenyl silanes, sulfones, phosphine oxides, and nitroolefins. In most cases, these radical substitutions a...
Gespeichert in:
Veröffentlicht in: | Organic letters 2017-03, Vol.19 (5), p.1100-1103 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1103 |
---|---|
container_issue | 5 |
container_start_page | 1100 |
container_title | Organic letters |
container_volume | 19 |
creator | Lin, Ya-mei Lu, Guo-ping Wang, Rong-kang Yi, Wen-bin |
description | A radical-mediated approach has been introduced for the C–S bond activation of arylalkenyl sulfides. The protocol provides an efficient approach for the generation of various alkenes including alkenyl silanes, sulfones, phosphine oxides, and nitroolefins. In most cases, these radical substitutions are performed under metal-free conditions with stereospecificity. |
doi_str_mv | 10.1021/acs.orglett.7b00126 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1869118167</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1869118167</sourcerecordid><originalsourceid>FETCH-LOGICAL-a345t-a906824a779be3071928216ba6acdfd4b27f273f9d6a815f8c8d781e8ea7d1813</originalsourceid><addsrcrecordid>eNp9kc9O3DAQxi1UxL_yBEiVjz2wi-3sxs4RVkArIaia9hxN4jFr6o0XO0HkxitUfcM-SR124djTjEa_7xvNfISccDblTPAzaOLUh3uHXTeVNWNc5DvkgM9FNpFsLj689znbJ4cxPiQkTYo9si8ULwrO5QH5XXYY0Ed02HT2CWk5tN0So43UG3rufmE7OFpaBy3GU1r2zvjX7tvSx_XStkjvnq0eJ9Bqemu74L1DY9tI64F-B20bcHTx9-VPSS98QhYO4Qnu8dU_DA7ediTr0egj2TXgIh5v6xH5eXX5Y_FlcnN3_XVxfjOBbDbvJlCwXIkZSFnUmDHJC6EEz2vIodFGz2ohjZCZKXQOis-NapSWiqNCkJornh2RzxvfdfCPPcauWtnYoBsv9X2suMrTixTPZUKzDdoEH2NAU62DXUEYKs6qMYsqZVFts6i2WSTVp-2Cvl6hfte8PT8BZxtgVD_4PrTp3v9a_gPwdJsV</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1869118167</pqid></control><display><type>article</type><title>Stereoselective Synthesis of Alkenyl Silanes, Sulfones, Phosphine Oxides, and Nitroolefins by Radical C–S Bond Cleavage of Arylalkenyl Sulfides</title><source>American Chemical Society Publications</source><creator>Lin, Ya-mei ; Lu, Guo-ping ; Wang, Rong-kang ; Yi, Wen-bin</creator><creatorcontrib>Lin, Ya-mei ; Lu, Guo-ping ; Wang, Rong-kang ; Yi, Wen-bin</creatorcontrib><description>A radical-mediated approach has been introduced for the C–S bond activation of arylalkenyl sulfides. The protocol provides an efficient approach for the generation of various alkenes including alkenyl silanes, sulfones, phosphine oxides, and nitroolefins. In most cases, these radical substitutions are performed under metal-free conditions with stereospecificity.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/acs.orglett.7b00126</identifier><identifier>PMID: 28199117</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Organic letters, 2017-03, Vol.19 (5), p.1100-1103</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a345t-a906824a779be3071928216ba6acdfd4b27f273f9d6a815f8c8d781e8ea7d1813</citedby><cites>FETCH-LOGICAL-a345t-a906824a779be3071928216ba6acdfd4b27f273f9d6a815f8c8d781e8ea7d1813</cites><orcidid>0000-0003-4476-964X ; 0000-0003-4606-7668</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b00126$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.orglett.7b00126$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28199117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Ya-mei</creatorcontrib><creatorcontrib>Lu, Guo-ping</creatorcontrib><creatorcontrib>Wang, Rong-kang</creatorcontrib><creatorcontrib>Yi, Wen-bin</creatorcontrib><title>Stereoselective Synthesis of Alkenyl Silanes, Sulfones, Phosphine Oxides, and Nitroolefins by Radical C–S Bond Cleavage of Arylalkenyl Sulfides</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>A radical-mediated approach has been introduced for the C–S bond activation of arylalkenyl sulfides. The protocol provides an efficient approach for the generation of various alkenes including alkenyl silanes, sulfones, phosphine oxides, and nitroolefins. In most cases, these radical substitutions are performed under metal-free conditions with stereospecificity.</description><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kc9O3DAQxi1UxL_yBEiVjz2wi-3sxs4RVkArIaia9hxN4jFr6o0XO0HkxitUfcM-SR124djTjEa_7xvNfISccDblTPAzaOLUh3uHXTeVNWNc5DvkgM9FNpFsLj689znbJ4cxPiQkTYo9si8ULwrO5QH5XXYY0Ed02HT2CWk5tN0So43UG3rufmE7OFpaBy3GU1r2zvjX7tvSx_XStkjvnq0eJ9Bqemu74L1DY9tI64F-B20bcHTx9-VPSS98QhYO4Qnu8dU_DA7ediTr0egj2TXgIh5v6xH5eXX5Y_FlcnN3_XVxfjOBbDbvJlCwXIkZSFnUmDHJC6EEz2vIodFGz2ohjZCZKXQOis-NapSWiqNCkJornh2RzxvfdfCPPcauWtnYoBsv9X2suMrTixTPZUKzDdoEH2NAU62DXUEYKs6qMYsqZVFts6i2WSTVp-2Cvl6hfte8PT8BZxtgVD_4PrTp3v9a_gPwdJsV</recordid><startdate>20170303</startdate><enddate>20170303</enddate><creator>Lin, Ya-mei</creator><creator>Lu, Guo-ping</creator><creator>Wang, Rong-kang</creator><creator>Yi, Wen-bin</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4476-964X</orcidid><orcidid>https://orcid.org/0000-0003-4606-7668</orcidid></search><sort><creationdate>20170303</creationdate><title>Stereoselective Synthesis of Alkenyl Silanes, Sulfones, Phosphine Oxides, and Nitroolefins by Radical C–S Bond Cleavage of Arylalkenyl Sulfides</title><author>Lin, Ya-mei ; Lu, Guo-ping ; Wang, Rong-kang ; Yi, Wen-bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a345t-a906824a779be3071928216ba6acdfd4b27f273f9d6a815f8c8d781e8ea7d1813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Ya-mei</creatorcontrib><creatorcontrib>Lu, Guo-ping</creatorcontrib><creatorcontrib>Wang, Rong-kang</creatorcontrib><creatorcontrib>Yi, Wen-bin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Ya-mei</au><au>Lu, Guo-ping</au><au>Wang, Rong-kang</au><au>Yi, Wen-bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stereoselective Synthesis of Alkenyl Silanes, Sulfones, Phosphine Oxides, and Nitroolefins by Radical C–S Bond Cleavage of Arylalkenyl Sulfides</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2017-03-03</date><risdate>2017</risdate><volume>19</volume><issue>5</issue><spage>1100</spage><epage>1103</epage><pages>1100-1103</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>A radical-mediated approach has been introduced for the C–S bond activation of arylalkenyl sulfides. The protocol provides an efficient approach for the generation of various alkenes including alkenyl silanes, sulfones, phosphine oxides, and nitroolefins. In most cases, these radical substitutions are performed under metal-free conditions with stereospecificity.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>28199117</pmid><doi>10.1021/acs.orglett.7b00126</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0003-4476-964X</orcidid><orcidid>https://orcid.org/0000-0003-4606-7668</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1523-7060 |
ispartof | Organic letters, 2017-03, Vol.19 (5), p.1100-1103 |
issn | 1523-7060 1523-7052 |
language | eng |
recordid | cdi_proquest_miscellaneous_1869118167 |
source | American Chemical Society Publications |
title | Stereoselective Synthesis of Alkenyl Silanes, Sulfones, Phosphine Oxides, and Nitroolefins by Radical C–S Bond Cleavage of Arylalkenyl Sulfides |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T05%3A36%3A21IST&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=Stereoselective%20Synthesis%20of%20Alkenyl%20Silanes,%20Sulfones,%20Phosphine%20Oxides,%20and%20Nitroolefins%20by%20Radical%20C%E2%80%93S%20Bond%20Cleavage%20of%20Arylalkenyl%20Sulfides&rft.jtitle=Organic%20letters&rft.au=Lin,%20Ya-mei&rft.date=2017-03-03&rft.volume=19&rft.issue=5&rft.spage=1100&rft.epage=1103&rft.pages=1100-1103&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/acs.orglett.7b00126&rft_dat=%3Cproquest_cross%3E1869118167%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=1869118167&rft_id=info:pmid/28199117&rfr_iscdi=true |