Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate
The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenien...
Gespeichert in:
Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2015-03, Vol.51 (21), p.4394-4397 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4397 |
---|---|
container_issue | 21 |
container_start_page | 4394 |
container_title | Chemical communications (Cambridge, England) |
container_volume | 51 |
creator | Lefebvre, Quentin Pluta, Roman Rueping, Magnus |
description | The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenient one-pot reaction, a scale up procedure as well as an extension to perfluoroalkylselenates are also presented to further demonstrate the synthetic utility of this reaction. |
doi_str_mv | 10.1039/c4cc10212f |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1659767591</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1659767591</sourcerecordid><originalsourceid>FETCH-LOGICAL-p211t-26d869356e6de312d8a92708dd90dfa644db1dddfef32a7a8a5fb38fda4e85b13</originalsourceid><addsrcrecordid>eNptkMtKxDAUhoMgzji68QEkSzfVpuklXUrxBgOCF3BXTpsTJ5I2NUnF-kq-pDPOuPPfHH74-A78hJyw-JzFvLxo07ZlccIStUfmjOdplKXiZUYOvX-L12GZOCCzJMuLrBTpnHxXdhjQ0RYCmOkLJbWfWkLQH0hbOw5G96_UIbRB295TZR0NTiszWmc7DKvJeDTYWwO_QBT5qQ8r9NpTq-hD9IjVNV-busGOvfR09BshaEd9gMYgDRgcbE3QdbbXY_fvBwh4RPYVrNvx7i7I8_XVU3UbLe9v7qrLZTQkjIUoyaXIS57lmEvkLJECyqSIhZRlLBXkaSobJqVUqHgCBQjIVMOFkpCiyBrGF-Rs6x2cfR_Rh7rTvkVjoEc7-prlWVlsBtygpzt0bDqU9eB0B26q_wbmPx9WgqU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1659767591</pqid></control><display><type>article</type><title>Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Lefebvre, Quentin ; Pluta, Roman ; Rueping, Magnus</creator><creatorcontrib>Lefebvre, Quentin ; Pluta, Roman ; Rueping, Magnus</creatorcontrib><description>The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenient one-pot reaction, a scale up procedure as well as an extension to perfluoroalkylselenates are also presented to further demonstrate the synthetic utility of this reaction.</description><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c4cc10212f</identifier><identifier>PMID: 25675984</identifier><language>eng</language><publisher>England</publisher><ispartof>Chemical communications (Cambridge, England), 2015-03, Vol.51 (21), p.4394-4397</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/25675984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lefebvre, Quentin</creatorcontrib><creatorcontrib>Pluta, Roman</creatorcontrib><creatorcontrib>Rueping, Magnus</creatorcontrib><title>Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenient one-pot reaction, a scale up procedure as well as an extension to perfluoroalkylselenates are also presented to further demonstrate the synthetic utility of this reaction.</description><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNptkMtKxDAUhoMgzji68QEkSzfVpuklXUrxBgOCF3BXTpsTJ5I2NUnF-kq-pDPOuPPfHH74-A78hJyw-JzFvLxo07ZlccIStUfmjOdplKXiZUYOvX-L12GZOCCzJMuLrBTpnHxXdhjQ0RYCmOkLJbWfWkLQH0hbOw5G96_UIbRB295TZR0NTiszWmc7DKvJeDTYWwO_QBT5qQ8r9NpTq-hD9IjVNV-busGOvfR09BshaEd9gMYgDRgcbE3QdbbXY_fvBwh4RPYVrNvx7i7I8_XVU3UbLe9v7qrLZTQkjIUoyaXIS57lmEvkLJECyqSIhZRlLBXkaSobJqVUqHgCBQjIVMOFkpCiyBrGF-Rs6x2cfR_Rh7rTvkVjoEc7-prlWVlsBtygpzt0bDqU9eB0B26q_wbmPx9WgqU</recordid><startdate>20150314</startdate><enddate>20150314</enddate><creator>Lefebvre, Quentin</creator><creator>Pluta, Roman</creator><creator>Rueping, Magnus</creator><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20150314</creationdate><title>Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate</title><author>Lefebvre, Quentin ; Pluta, Roman ; Rueping, Magnus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-26d869356e6de312d8a92708dd90dfa644db1dddfef32a7a8a5fb38fda4e85b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lefebvre, Quentin</creatorcontrib><creatorcontrib>Pluta, Roman</creatorcontrib><creatorcontrib>Rueping, Magnus</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lefebvre, Quentin</au><au>Pluta, Roman</au><au>Rueping, Magnus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2015-03-14</date><risdate>2015</risdate><volume>51</volume><issue>21</issue><spage>4394</spage><epage>4397</epage><pages>4394-4397</pages><eissn>1364-548X</eissn><abstract>The aerobic, room-temperature coupling of tetramethylammonium trifluoromethylselenate with readily available boronic acids, boronic esters, and terminal alkynes has been developed. The method permits direct access to valuable trifluoromethylselenoarenes and alkynes under mild conditions. A convenient one-pot reaction, a scale up procedure as well as an extension to perfluoroalkylselenates are also presented to further demonstrate the synthetic utility of this reaction.</abstract><cop>England</cop><pmid>25675984</pmid><doi>10.1039/c4cc10212f</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1364-548X |
ispartof | Chemical communications (Cambridge, England), 2015-03, Vol.51 (21), p.4394-4397 |
issn | 1364-548X |
language | eng |
recordid | cdi_proquest_miscellaneous_1659767591 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Copper catalyzed oxidative coupling reactions for trifluoromethylselenolations--synthesis of R-SeCF3 compounds using air stable tetramethylammonium trifluoromethylselenate |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T10%3A09%3A42IST&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=Copper%20catalyzed%20oxidative%20coupling%20reactions%20for%20trifluoromethylselenolations--synthesis%20of%20R-SeCF3%20compounds%20using%20air%20stable%20tetramethylammonium%20trifluoromethylselenate&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Lefebvre,%20Quentin&rft.date=2015-03-14&rft.volume=51&rft.issue=21&rft.spage=4394&rft.epage=4397&rft.pages=4394-4397&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c4cc10212f&rft_dat=%3Cproquest_pubme%3E1659767591%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=1659767591&rft_id=info:pmid/25675984&rfr_iscdi=true |