Cross-Coupling Reactions of Potassium Alkyltrifluoroborates with Aryl and 1-Alkenyl Trifluoromethanesulfonates
The palladium-catalyzed coupling reaction of potassium alkyltrifluoroborates with aryl- or alkenyltriflates proceeds to afford the corresponding arenes or alkenes in high yield. The borates are all solids, stable in air, and thus can be stored on the shelf indefinitely. The cross coupling can be eff...
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Veröffentlicht in: | Organic letters 2001-02, Vol.3 (3), p.393-396 |
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creator | Molander, Gary A Ito, Takatoshi |
description | The palladium-catalyzed coupling reaction of potassium alkyltrifluoroborates with aryl- or alkenyltriflates proceeds to afford the corresponding arenes or alkenes in high yield. The borates are all solids, stable in air, and thus can be stored on the shelf indefinitely. The cross coupling can be effected using PdCl2(dppf)·CH2Cl2 as the catalyst in THF−H2O in the presence of Cs2CO3. A variety of functional groups can be tolerated within the borate and/or the triflate coupling partner. |
doi_str_mv | 10.1021/ol006896u |
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The borates are all solids, stable in air, and thus can be stored on the shelf indefinitely. The cross coupling can be effected using PdCl2(dppf)·CH2Cl2 as the catalyst in THF−H2O in the presence of Cs2CO3. A variety of functional groups can be tolerated within the borate and/or the triflate coupling partner.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol006896u</identifier><identifier>PMID: 11428022</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Alkenes - chemical synthesis ; Borates - chemistry ; Mesylates - chemistry</subject><ispartof>Organic letters, 2001-02, Vol.3 (3), p.393-396</ispartof><rights>Copyright © 2001 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a311t-92d1ebf55911795c398d0e51f0fa328c592ed47ea1aa12fa89a7ce5896ae7f2f3</citedby><cites>FETCH-LOGICAL-a311t-92d1ebf55911795c398d0e51f0fa328c592ed47ea1aa12fa89a7ce5896ae7f2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ol006896u$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ol006896u$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,778,782,2754,27063,27911,27912,56725,56775</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11428022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Molander, Gary A</creatorcontrib><creatorcontrib>Ito, Takatoshi</creatorcontrib><title>Cross-Coupling Reactions of Potassium Alkyltrifluoroborates with Aryl and 1-Alkenyl Trifluoromethanesulfonates</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>The palladium-catalyzed coupling reaction of potassium alkyltrifluoroborates with aryl- or alkenyltriflates proceeds to afford the corresponding arenes or alkenes in high yield. The borates are all solids, stable in air, and thus can be stored on the shelf indefinitely. The cross coupling can be effected using PdCl2(dppf)·CH2Cl2 as the catalyst in THF−H2O in the presence of Cs2CO3. A variety of functional groups can be tolerated within the borate and/or the triflate coupling partner.</description><subject>Alkenes - chemical synthesis</subject><subject>Borates - chemistry</subject><subject>Mesylates - chemistry</subject><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1LAzEQhoMotlYP_gHJRcHDaibbdJNjWfwCQZF6XtLdxG7Nbmo-kP57U1rrxVMmwzMvMw9C50BugFC4tYaQCReTeICGwGieFYTRw309IQN04v2SEEgdcYwGAGPKCaVD1JfOep-VNq5M23_gNyXr0NreY6vxqw3S-zZ2eGo-1ya4VptonZ1bJ4Py-LsNCzx1a4Nl32DIEqX69Jv9gp0KC9krH422_WbkFB1pabw6270j9H5_Nysfs-eXh6dy-pzJHCBkgjag5poxAVAIVueCN0Qx0ETLnPKaCaqacaEkSAlUSy5kUSuWFEhVaKrzEbra5q6c_YrKh6prfa2MSdvY6KuCiAnngifwegvWGw9O6Wrl2k66dQWk2sit9nITe7ELjfNONX_kzmYCLreArH21tNH16cZ_gn4A0HeDnA</recordid><startdate>20010208</startdate><enddate>20010208</enddate><creator>Molander, Gary A</creator><creator>Ito, Takatoshi</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20010208</creationdate><title>Cross-Coupling Reactions of Potassium Alkyltrifluoroborates with Aryl and 1-Alkenyl Trifluoromethanesulfonates</title><author>Molander, Gary A ; Ito, Takatoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a311t-92d1ebf55911795c398d0e51f0fa328c592ed47ea1aa12fa89a7ce5896ae7f2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Alkenes - chemical synthesis</topic><topic>Borates - chemistry</topic><topic>Mesylates - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Molander, Gary A</creatorcontrib><creatorcontrib>Ito, Takatoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><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>Molander, Gary A</au><au>Ito, Takatoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cross-Coupling Reactions of Potassium Alkyltrifluoroborates with Aryl and 1-Alkenyl Trifluoromethanesulfonates</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2001-02-08</date><risdate>2001</risdate><volume>3</volume><issue>3</issue><spage>393</spage><epage>396</epage><pages>393-396</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>The palladium-catalyzed coupling reaction of potassium alkyltrifluoroborates with aryl- or alkenyltriflates proceeds to afford the corresponding arenes or alkenes in high yield. The borates are all solids, stable in air, and thus can be stored on the shelf indefinitely. The cross coupling can be effected using PdCl2(dppf)·CH2Cl2 as the catalyst in THF−H2O in the presence of Cs2CO3. A variety of functional groups can be tolerated within the borate and/or the triflate coupling partner.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>11428022</pmid><doi>10.1021/ol006896u</doi><tpages>4</tpages></addata></record> |
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subjects | Alkenes - chemical synthesis Borates - chemistry Mesylates - chemistry |
title | Cross-Coupling Reactions of Potassium Alkyltrifluoroborates with Aryl and 1-Alkenyl Trifluoromethanesulfonates |
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