Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters
An approach for the palladium‐catalyzed ethoxycarbonylations of arylboronic acids using diethyl pyrocarbonate as carbon monoxide/carbon dioxide (CO/CO2) surrogate in moderate to good yields has been investigated.
Gespeichert in:
| Veröffentlicht in: | Advanced synthesis & catalysis 2015-10, Vol.357 (14-15), p.3104-3108 |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 3108 |
|---|---|
| container_issue | 14-15 |
| container_start_page | 3104 |
| container_title | Advanced synthesis & catalysis |
| container_volume | 357 |
| creator | Liang, Apeng Han, Shuaijun Wang, Liang Li, Jingya Zou, Dapeng Wu, Yangjie Wu, Yusheng |
| description | An approach for the palladium‐catalyzed ethoxycarbonylations of arylboronic acids using diethyl pyrocarbonate as carbon monoxide/carbon dioxide (CO/CO2) surrogate in moderate to good yields has been investigated. |
| doi_str_mv | 10.1002/adsc.201500521 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1770287538</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1770287538</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4631-b28d9a3e76e58fc857e62c6b5cdee6c8da5a871352940a9fdc2d117a1e93da363</originalsourceid><addsrcrecordid>eNqFkM9LwzAYQIsoOKdXzz166Uya5Ue9jTqnsE1hiseQJimLZu1MOlz86-3oKN485YO898H3ougaghEEIL0VystRCiAGAKfwJBpAAnEyhiQ77WcMzqML7z8AgJRROojKF2GtUGa3SXLRCBt-tIpz4Yq6ClY0pq58XJfxxAVb1K6ujIwn0ih_F69C1ay1N_2_PFj7YI9IPG3WwcZT32jnL6OzUlivr47vMHp7mL7mj8n8efaUT-aJHBMEkyJlKhNIU6IxKyXDVJNUkgJLpTWRTAksGIUIp9kYiKxUMlUQUgF1hpRABA2jm27v1tVfO-0bvjFe6vbEStc7zyGlIGUUI9aiow6Vrvbe6ZJvndkIFzgE_BCUH4LyPmgrZJ3wbawO_9B8cr_K_7pJ55o2x753hfvkhCKK-ftyxudLNlssFowD9AtteYq4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1770287538</pqid></control><display><type>article</type><title>Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Liang, Apeng ; Han, Shuaijun ; Wang, Liang ; Li, Jingya ; Zou, Dapeng ; Wu, Yangjie ; Wu, Yusheng</creator><creatorcontrib>Liang, Apeng ; Han, Shuaijun ; Wang, Liang ; Li, Jingya ; Zou, Dapeng ; Wu, Yangjie ; Wu, Yusheng</creatorcontrib><description>An approach for the palladium‐catalyzed ethoxycarbonylations of arylboronic acids using diethyl pyrocarbonate as carbon monoxide/carbon dioxide (CO/CO2) surrogate in moderate to good yields has been investigated.</description><identifier>ISSN: 1615-4150</identifier><identifier>EISSN: 1615-4169</identifier><identifier>DOI: 10.1002/adsc.201500521</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>arylboronic acids ; arylcarboxylic acid ethyl esters ; Carbon dioxide ; Carbon monoxide ; Carbonyls ; Catalysis ; CO/CO2 surrogate ; diethyl pyrocarbonate ; Ethyl esters ; palladium-catalyzed carbonylation ; Synthesis</subject><ispartof>Advanced synthesis & catalysis, 2015-10, Vol.357 (14-15), p.3104-3108</ispartof><rights>2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4631-b28d9a3e76e58fc857e62c6b5cdee6c8da5a871352940a9fdc2d117a1e93da363</citedby><cites>FETCH-LOGICAL-c4631-b28d9a3e76e58fc857e62c6b5cdee6c8da5a871352940a9fdc2d117a1e93da363</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%2Fadsc.201500521$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadsc.201500521$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids></links><search><creatorcontrib>Liang, Apeng</creatorcontrib><creatorcontrib>Han, Shuaijun</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Li, Jingya</creatorcontrib><creatorcontrib>Zou, Dapeng</creatorcontrib><creatorcontrib>Wu, Yangjie</creatorcontrib><creatorcontrib>Wu, Yusheng</creatorcontrib><title>Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters</title><title>Advanced synthesis & catalysis</title><addtitle>Adv. Synth. Catal</addtitle><description>An approach for the palladium‐catalyzed ethoxycarbonylations of arylboronic acids using diethyl pyrocarbonate as carbon monoxide/carbon dioxide (CO/CO2) surrogate in moderate to good yields has been investigated.</description><subject>arylboronic acids</subject><subject>arylcarboxylic acid ethyl esters</subject><subject>Carbon dioxide</subject><subject>Carbon monoxide</subject><subject>Carbonyls</subject><subject>Catalysis</subject><subject>CO/CO2 surrogate</subject><subject>diethyl pyrocarbonate</subject><subject>Ethyl esters</subject><subject>palladium-catalyzed carbonylation</subject><subject>Synthesis</subject><issn>1615-4150</issn><issn>1615-4169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkM9LwzAYQIsoOKdXzz166Uya5Ue9jTqnsE1hiseQJimLZu1MOlz86-3oKN485YO898H3ougaghEEIL0VystRCiAGAKfwJBpAAnEyhiQ77WcMzqML7z8AgJRROojKF2GtUGa3SXLRCBt-tIpz4Yq6ClY0pq58XJfxxAVb1K6ujIwn0ih_F69C1ay1N_2_PFj7YI9IPG3WwcZT32jnL6OzUlivr47vMHp7mL7mj8n8efaUT-aJHBMEkyJlKhNIU6IxKyXDVJNUkgJLpTWRTAksGIUIp9kYiKxUMlUQUgF1hpRABA2jm27v1tVfO-0bvjFe6vbEStc7zyGlIGUUI9aiow6Vrvbe6ZJvndkIFzgE_BCUH4LyPmgrZJ3wbawO_9B8cr_K_7pJ55o2x753hfvkhCKK-ftyxudLNlssFowD9AtteYq4</recordid><startdate>20151012</startdate><enddate>20151012</enddate><creator>Liang, Apeng</creator><creator>Han, Shuaijun</creator><creator>Wang, Liang</creator><creator>Li, Jingya</creator><creator>Zou, Dapeng</creator><creator>Wu, Yangjie</creator><creator>Wu, Yusheng</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20151012</creationdate><title>Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters</title><author>Liang, Apeng ; Han, Shuaijun ; Wang, Liang ; Li, Jingya ; Zou, Dapeng ; Wu, Yangjie ; Wu, Yusheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4631-b28d9a3e76e58fc857e62c6b5cdee6c8da5a871352940a9fdc2d117a1e93da363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>arylboronic acids</topic><topic>arylcarboxylic acid ethyl esters</topic><topic>Carbon dioxide</topic><topic>Carbon monoxide</topic><topic>Carbonyls</topic><topic>Catalysis</topic><topic>CO/CO2 surrogate</topic><topic>diethyl pyrocarbonate</topic><topic>Ethyl esters</topic><topic>palladium-catalyzed carbonylation</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liang, Apeng</creatorcontrib><creatorcontrib>Han, Shuaijun</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Li, Jingya</creatorcontrib><creatorcontrib>Zou, Dapeng</creatorcontrib><creatorcontrib>Wu, Yangjie</creatorcontrib><creatorcontrib>Wu, Yusheng</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced synthesis & catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Apeng</au><au>Han, Shuaijun</au><au>Wang, Liang</au><au>Li, Jingya</au><au>Zou, Dapeng</au><au>Wu, Yangjie</au><au>Wu, Yusheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters</atitle><jtitle>Advanced synthesis & catalysis</jtitle><addtitle>Adv. Synth. Catal</addtitle><date>2015-10-12</date><risdate>2015</risdate><volume>357</volume><issue>14-15</issue><spage>3104</spage><epage>3108</epage><pages>3104-3108</pages><issn>1615-4150</issn><eissn>1615-4169</eissn><abstract>An approach for the palladium‐catalyzed ethoxycarbonylations of arylboronic acids using diethyl pyrocarbonate as carbon monoxide/carbon dioxide (CO/CO2) surrogate in moderate to good yields has been investigated.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/adsc.201500521</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1615-4150 |
| ispartof | Advanced synthesis & catalysis, 2015-10, Vol.357 (14-15), p.3104-3108 |
| issn | 1615-4150 1615-4169 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1770287538 |
| source | Wiley Online Library Journals Frontfile Complete |
| subjects | arylboronic acids arylcarboxylic acid ethyl esters Carbon dioxide Carbon monoxide Carbonyls Catalysis CO/CO2 surrogate diethyl pyrocarbonate Ethyl esters palladium-catalyzed carbonylation Synthesis |
| title | Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T13%3A29%3A25IST&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=Palladium-Catalyzed%20Carbonylations%20of%20Arylboronic%20Acids:%20Synthesis%20of%20Arylcarboxylic%20Acid%20Ethyl%20Esters&rft.jtitle=Advanced%20synthesis%20&%20catalysis&rft.au=Liang,%20Apeng&rft.date=2015-10-12&rft.volume=357&rft.issue=14-15&rft.spage=3104&rft.epage=3108&rft.pages=3104-3108&rft.issn=1615-4150&rft.eissn=1615-4169&rft_id=info:doi/10.1002/adsc.201500521&rft_dat=%3Cproquest_cross%3E1770287538%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=1770287538&rft_id=info:pmid/&rfr_iscdi=true |