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Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source
An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing...
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Published in: | Angewandte Chemie International Edition 2016-07, Vol.55 (30), p.8740-8743 |
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creator | Kawamura, Shintaro Sodeoka, Mikiko |
description | An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing an aromatic ring at an appropriate position on the carbon side chain was found to proceed under metal‐free conditions to afford carbocycles or heterocycles bearing a perfluoroalkyl group. This method, which makes use of readily available perfluoroalkyl sources, offers a convenient and powerful tool for introducing a perfluoroalkyl group onto an sp3 carbon to construct synthetically useful skeletons.
F for effective: Perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides as the perfluoroalkyl source was achieved. A copper catalyst enabled efficient allylic perfluoroalkylation with in situ generated diacyl peroxide. In addition, alkenes bearing an aromatic ring at an appropriate position on the carbon side chain afforded carboperfluoroalkylation products under metal‐free conditions. |
doi_str_mv | 10.1002/anie.201604127 |
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F for effective: Perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides as the perfluoroalkyl source was achieved. A copper catalyst enabled efficient allylic perfluoroalkylation with in situ generated diacyl peroxide. In addition, alkenes bearing an aromatic ring at an appropriate position on the carbon side chain afforded carboperfluoroalkylation products under metal‐free conditions.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201604127</identifier><identifier>PMID: 27254318</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>alkenes ; copper ; homogeneous catalysis ; perfluoroalkylation ; peroxide</subject><ispartof>Angewandte Chemie International Edition, 2016-07, Vol.55 (30), p.8740-8743</ispartof><rights>2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4487-7c65c49b525947cb1d7ea726f65f00fe9b9ed80239bdcd0998a740dc2e585f9b3</citedby><cites>FETCH-LOGICAL-c4487-7c65c49b525947cb1d7ea726f65f00fe9b9ed80239bdcd0998a740dc2e585f9b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27254318$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawamura, Shintaro</creatorcontrib><creatorcontrib>Sodeoka, Mikiko</creatorcontrib><title>Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing an aromatic ring at an appropriate position on the carbon side chain was found to proceed under metal‐free conditions to afford carbocycles or heterocycles bearing a perfluoroalkyl group. This method, which makes use of readily available perfluoroalkyl sources, offers a convenient and powerful tool for introducing a perfluoroalkyl group onto an sp3 carbon to construct synthetically useful skeletons.
F for effective: Perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides as the perfluoroalkyl source was achieved. A copper catalyst enabled efficient allylic perfluoroalkylation with in situ generated diacyl peroxide. In addition, alkenes bearing an aromatic ring at an appropriate position on the carbon side chain afforded carboperfluoroalkylation products under metal‐free conditions.</description><subject>alkenes</subject><subject>copper</subject><subject>homogeneous catalysis</subject><subject>perfluoroalkylation</subject><subject>peroxide</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PGzEQhi1EVSjtlSNaiUsvm_pzbR-jiFIQokgNpYdKlteeVUw2u2Dvlubf11FoRHvhNKPR8z4avQgdEzwhGNNPtgswoZhUmBMq99AhEZSUTEq2n3fOWCmVIAfoXUr3mVcKV2_RAZVUcEbUIfp5A7Fpxz72tl2uWzuEviv6prjtrBvCLzuAL6btEjpIxVMYFsXUhXzpFmsfg89Hm4phAcW_muJbP0YH79GbxrYJPjzPI3T7-Ww--1JefT2_mE2vSse5kqV0lXBc14IKzaWriZdgJa2aSjQYN6BrDV5hynTtncdaKys59o6CUKLRNTtCH7feh9g_jpAGswrJQdvaDvoxGaIwV4LjimT09D_0Pr_a5e82FBOcc7qhJlvKxT6lCI15iGFl49oQbDa9m03vZtd7Dpw8a8d6BX6H_y06A3oLPIUW1q_ozPT64uylvNxmQxrg9y5r49JUkklh7q7PzfzH5fz7pbozM_YHtGaeoA</recordid><startdate>20160718</startdate><enddate>20160718</enddate><creator>Kawamura, Shintaro</creator><creator>Sodeoka, Mikiko</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20160718</creationdate><title>Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source</title><author>Kawamura, Shintaro ; Sodeoka, Mikiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4487-7c65c49b525947cb1d7ea726f65f00fe9b9ed80239bdcd0998a740dc2e585f9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>alkenes</topic><topic>copper</topic><topic>homogeneous catalysis</topic><topic>perfluoroalkylation</topic><topic>peroxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawamura, Shintaro</creatorcontrib><creatorcontrib>Sodeoka, Mikiko</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawamura, Shintaro</au><au>Sodeoka, Mikiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2016-07-18</date><risdate>2016</risdate><volume>55</volume><issue>30</issue><spage>8740</spage><epage>8743</epage><pages>8740-8743</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing an aromatic ring at an appropriate position on the carbon side chain was found to proceed under metal‐free conditions to afford carbocycles or heterocycles bearing a perfluoroalkyl group. This method, which makes use of readily available perfluoroalkyl sources, offers a convenient and powerful tool for introducing a perfluoroalkyl group onto an sp3 carbon to construct synthetically useful skeletons.
F for effective: Perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides as the perfluoroalkyl source was achieved. A copper catalyst enabled efficient allylic perfluoroalkylation with in situ generated diacyl peroxide. In addition, alkenes bearing an aromatic ring at an appropriate position on the carbon side chain afforded carboperfluoroalkylation products under metal‐free conditions.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>27254318</pmid><doi>10.1002/anie.201604127</doi><tpages>4</tpages><edition>International ed. in English</edition></addata></record> |
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subjects | alkenes copper homogeneous catalysis perfluoroalkylation peroxide |
title | Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source |
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