A Carbocyclic Carbene as an Efficient Catalyst Ligand for CC Coupling Reactions
A new player on the field: Carbocyclic carbenes are potentially better control ligands than N‐heterocyclic carbenes (NHCs) in catalyzed CC coupling reactions. PdII complexes of cycloheptatrienylidene (see picture), which are readily prepared, thermally stable, and highly stable towards acid, are as...
Gespeichert in:
Veröffentlicht in: | Angewandte Chemie International Edition 2006-06, Vol.45 (23), p.3859-3862 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3862 |
---|---|
container_issue | 23 |
container_start_page | 3859 |
container_title | Angewandte Chemie International Edition |
container_volume | 45 |
creator | Herrmann, Wolfgang A. Öfele, Karl Schneider, Sabine K. Herdtweck, Eberhardt Hoffmann, Stephan D. |
description | A new player on the field: Carbocyclic carbenes are potentially better control ligands than N‐heterocyclic carbenes (NHCs) in catalyzed CC coupling reactions. PdII complexes of cycloheptatrienylidene (see picture), which are readily prepared, thermally stable, and highly stable towards acid, are as effective as the familiar NHC complexes in Suzuki and Heck reactions or perform even better. |
doi_str_mv | 10.1002/anie.200503589 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68028611</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68028611</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4479-82462d2e058d2db2622ef0835c8eaf29f298484ea51e29907eb7139589044cc53</originalsourceid><addsrcrecordid>eNqFkM1Kw0AUhQdR_N-6lFm5S53fzGRZQq1KqVgUl8N0ciOjaVIzKdrn8UF8JF_BqS3qTrhwL5fvHDgHoRNKepQQdm5rDz1GiCRc6mwL7VPJaMKV4tvxFpwnSku6hw5CeIq81iTdRXs0TRWlQu2jSR_ntp02bukq775vqAHbgG2NB2XpnYe6i__OVsvQ4ZF_tHWBy6bF-ef7R47zZjGvfP2IJ2Bd55s6HKGd0lYBjjf7EN1fDO7yy2R0M7zK-6PECaGyRDORsoIBkbpgxZSljEFJNJdOgy1ZFkcLLcBKCizLiIKpojyLKYkQzkl-iM7WvvO2eVlA6MzMBwdVZWtoFsGkOuZNKY1gbw26tgmhhdLMWz-z7dJQYlYtmlWL5qfFKDjdOC-mMyh-8U1tEcjWwKuvYPmPnemPrwZ_zZO11ocO3n60tn02qeJKmofx0Azl8PqWUG0U_wLBp4yS</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68028611</pqid></control><display><type>article</type><title>A Carbocyclic Carbene as an Efficient Catalyst Ligand for CC Coupling Reactions</title><source>Wiley Online Library All Journals</source><creator>Herrmann, Wolfgang A. ; Öfele, Karl ; Schneider, Sabine K. ; Herdtweck, Eberhardt ; Hoffmann, Stephan D.</creator><creatorcontrib>Herrmann, Wolfgang A. ; Öfele, Karl ; Schneider, Sabine K. ; Herdtweck, Eberhardt ; Hoffmann, Stephan D.</creatorcontrib><description>A new player on the field: Carbocyclic carbenes are potentially better control ligands than N‐heterocyclic carbenes (NHCs) in catalyzed CC coupling reactions. PdII complexes of cycloheptatrienylidene (see picture), which are readily prepared, thermally stable, and highly stable towards acid, are as effective as the familiar NHC complexes in Suzuki and Heck reactions or perform even better.</description><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.200503589</identifier><identifier>PMID: 16671147</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>carbenes ; carbocycles ; CC coupling ; homogeneous catalysis ; palladium</subject><ispartof>Angewandte Chemie International Edition, 2006-06, Vol.45 (23), p.3859-3862</ispartof><rights>Copyright © 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4479-82462d2e058d2db2622ef0835c8eaf29f298484ea51e29907eb7139589044cc53</citedby><cites>FETCH-LOGICAL-c4479-82462d2e058d2db2622ef0835c8eaf29f298484ea51e29907eb7139589044cc53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.200503589$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.200503589$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16671147$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Herrmann, Wolfgang A.</creatorcontrib><creatorcontrib>Öfele, Karl</creatorcontrib><creatorcontrib>Schneider, Sabine K.</creatorcontrib><creatorcontrib>Herdtweck, Eberhardt</creatorcontrib><creatorcontrib>Hoffmann, Stephan D.</creatorcontrib><title>A Carbocyclic Carbene as an Efficient Catalyst Ligand for CC Coupling Reactions</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>A new player on the field: Carbocyclic carbenes are potentially better control ligands than N‐heterocyclic carbenes (NHCs) in catalyzed CC coupling reactions. PdII complexes of cycloheptatrienylidene (see picture), which are readily prepared, thermally stable, and highly stable towards acid, are as effective as the familiar NHC complexes in Suzuki and Heck reactions or perform even better.</description><subject>carbenes</subject><subject>carbocycles</subject><subject>CC coupling</subject><subject>homogeneous catalysis</subject><subject>palladium</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkM1Kw0AUhQdR_N-6lFm5S53fzGRZQq1KqVgUl8N0ciOjaVIzKdrn8UF8JF_BqS3qTrhwL5fvHDgHoRNKepQQdm5rDz1GiCRc6mwL7VPJaMKV4tvxFpwnSku6hw5CeIq81iTdRXs0TRWlQu2jSR_ntp02bukq775vqAHbgG2NB2XpnYe6i__OVsvQ4ZF_tHWBy6bF-ef7R47zZjGvfP2IJ2Bd55s6HKGd0lYBjjf7EN1fDO7yy2R0M7zK-6PECaGyRDORsoIBkbpgxZSljEFJNJdOgy1ZFkcLLcBKCizLiIKpojyLKYkQzkl-iM7WvvO2eVlA6MzMBwdVZWtoFsGkOuZNKY1gbw26tgmhhdLMWz-z7dJQYlYtmlWL5qfFKDjdOC-mMyh-8U1tEcjWwKuvYPmPnemPrwZ_zZO11ocO3n60tn02qeJKmofx0Azl8PqWUG0U_wLBp4yS</recordid><startdate>20060602</startdate><enddate>20060602</enddate><creator>Herrmann, Wolfgang A.</creator><creator>Öfele, Karl</creator><creator>Schneider, Sabine K.</creator><creator>Herdtweck, Eberhardt</creator><creator>Hoffmann, Stephan D.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060602</creationdate><title>A Carbocyclic Carbene as an Efficient Catalyst Ligand for CC Coupling Reactions</title><author>Herrmann, Wolfgang A. ; Öfele, Karl ; Schneider, Sabine K. ; Herdtweck, Eberhardt ; Hoffmann, Stephan D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4479-82462d2e058d2db2622ef0835c8eaf29f298484ea51e29907eb7139589044cc53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>carbenes</topic><topic>carbocycles</topic><topic>CC coupling</topic><topic>homogeneous catalysis</topic><topic>palladium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herrmann, Wolfgang A.</creatorcontrib><creatorcontrib>Öfele, Karl</creatorcontrib><creatorcontrib>Schneider, Sabine K.</creatorcontrib><creatorcontrib>Herdtweck, Eberhardt</creatorcontrib><creatorcontrib>Hoffmann, Stephan D.</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herrmann, Wolfgang A.</au><au>Öfele, Karl</au><au>Schneider, Sabine K.</au><au>Herdtweck, Eberhardt</au><au>Hoffmann, Stephan D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Carbocyclic Carbene as an Efficient Catalyst Ligand for CC Coupling Reactions</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2006-06-02</date><risdate>2006</risdate><volume>45</volume><issue>23</issue><spage>3859</spage><epage>3862</epage><pages>3859-3862</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>A new player on the field: Carbocyclic carbenes are potentially better control ligands than N‐heterocyclic carbenes (NHCs) in catalyzed CC coupling reactions. PdII complexes of cycloheptatrienylidene (see picture), which are readily prepared, thermally stable, and highly stable towards acid, are as effective as the familiar NHC complexes in Suzuki and Heck reactions or perform even better.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>16671147</pmid><doi>10.1002/anie.200503589</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2006-06, Vol.45 (23), p.3859-3862 |
issn | 1433-7851 1521-3773 |
language | eng |
recordid | cdi_proquest_miscellaneous_68028611 |
source | Wiley Online Library All Journals |
subjects | carbenes carbocycles CC coupling homogeneous catalysis palladium |
title | A Carbocyclic Carbene as an Efficient Catalyst Ligand for CC Coupling Reactions |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T00%3A19%3A06IST&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=A%20Carbocyclic%20Carbene%20as%20an%20Efficient%20Catalyst%20Ligand%20for%20C%EF%A3%BFC%20Coupling%20Reactions&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Herrmann,%20Wolfgang%20A.&rft.date=2006-06-02&rft.volume=45&rft.issue=23&rft.spage=3859&rft.epage=3862&rft.pages=3859-3862&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.200503589&rft_dat=%3Cproquest_cross%3E68028611%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=68028611&rft_id=info:pmid/16671147&rfr_iscdi=true |