Highly Efficient Pd-Catalyzed Cyanation of Aryl Chlorides and Arenesulfonates with Potassium Ferrocyanide in Aqueous Media
A highly improved Pd-catalyzed cyanation of aryl chlorides to corresponding benzonitriles was demonstrated in aqueous media. Moreover, Pd-catalyzed cyanation of aryl tosylates and benzenesulfonates with K 4 [Fe(CN) 6 ] was developed under the similar conditions, which extended application scope of t...
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Veröffentlicht in: | Catalysis letters 2010-10, Vol.139 (1-2), p.56-60 |
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creator | Zhang, Junli Chen, Xiaorong Hu, Tongjie Zhang, Yuan Xu, Kunling Yu, Yanpeng Huang, Jun |
description | A highly improved Pd-catalyzed cyanation of aryl chlorides to corresponding benzonitriles was demonstrated in aqueous media. Moreover, Pd-catalyzed cyanation of aryl tosylates and benzenesulfonates with K
4
[Fe(CN)
6
] was developed under the similar conditions, which extended application scope of the cyanation.
Graphical Abstract |
doi_str_mv | 10.1007/s10562-010-0385-1 |
format | Article |
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4
[Fe(CN)
6
] was developed under the similar conditions, which extended application scope of the cyanation.
Graphical Abstract</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1007/s10562-010-0385-1</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Aqueous solutions ; Aromatic compounds ; Catalysis ; Chemistry ; Chemistry and Materials Science ; Chlorides ; Dichloropropane ; Exact sciences and technology ; General and physical chemistry ; Industrial Chemistry/Chemical Engineering ; Iron compounds ; Iron cyanides ; Nitriles ; Organometallic Chemistry ; Palladium ; Physical Chemistry ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Catalysis letters, 2010-10, Vol.139 (1-2), p.56-60</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 Springer</rights><rights>Catalysis Letters is a copyright of Springer, (2010). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-1cf9885347165c067d243ed3c856566b7b1887e70e4efe5b54be33d62b8ddb813</citedby><cites>FETCH-LOGICAL-c419t-1cf9885347165c067d243ed3c856566b7b1887e70e4efe5b54be33d62b8ddb813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10562-010-0385-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10562-010-0385-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23324011$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Junli</creatorcontrib><creatorcontrib>Chen, Xiaorong</creatorcontrib><creatorcontrib>Hu, Tongjie</creatorcontrib><creatorcontrib>Zhang, Yuan</creatorcontrib><creatorcontrib>Xu, Kunling</creatorcontrib><creatorcontrib>Yu, Yanpeng</creatorcontrib><creatorcontrib>Huang, Jun</creatorcontrib><title>Highly Efficient Pd-Catalyzed Cyanation of Aryl Chlorides and Arenesulfonates with Potassium Ferrocyanide in Aqueous Media</title><title>Catalysis letters</title><addtitle>Catal Lett</addtitle><description>A highly improved Pd-catalyzed cyanation of aryl chlorides to corresponding benzonitriles was demonstrated in aqueous media. Moreover, Pd-catalyzed cyanation of aryl tosylates and benzenesulfonates with K
4
[Fe(CN)
6
] was developed under the similar conditions, which extended application scope of the cyanation.
Graphical Abstract</description><subject>Aqueous solutions</subject><subject>Aromatic compounds</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chlorides</subject><subject>Dichloropropane</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Iron compounds</subject><subject>Iron cyanides</subject><subject>Nitriles</subject><subject>Organometallic Chemistry</subject><subject>Palladium</subject><subject>Physical Chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Junli</creatorcontrib><creatorcontrib>Chen, Xiaorong</creatorcontrib><creatorcontrib>Hu, Tongjie</creatorcontrib><creatorcontrib>Zhang, Yuan</creatorcontrib><creatorcontrib>Xu, Kunling</creatorcontrib><creatorcontrib>Yu, Yanpeng</creatorcontrib><creatorcontrib>Huang, Jun</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysis letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Junli</au><au>Chen, Xiaorong</au><au>Hu, Tongjie</au><au>Zhang, Yuan</au><au>Xu, Kunling</au><au>Yu, Yanpeng</au><au>Huang, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly Efficient Pd-Catalyzed Cyanation of Aryl Chlorides and Arenesulfonates with Potassium Ferrocyanide in Aqueous Media</atitle><jtitle>Catalysis letters</jtitle><stitle>Catal Lett</stitle><date>2010-10-01</date><risdate>2010</risdate><volume>139</volume><issue>1-2</issue><spage>56</spage><epage>60</epage><pages>56-60</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>A highly improved Pd-catalyzed cyanation of aryl chlorides to corresponding benzonitriles was demonstrated in aqueous media. Moreover, Pd-catalyzed cyanation of aryl tosylates and benzenesulfonates with K
4
[Fe(CN)
6
] was developed under the similar conditions, which extended application scope of the cyanation.
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subjects | Aqueous solutions Aromatic compounds Catalysis Chemistry Chemistry and Materials Science Chlorides Dichloropropane Exact sciences and technology General and physical chemistry Industrial Chemistry/Chemical Engineering Iron compounds Iron cyanides Nitriles Organometallic Chemistry Palladium Physical Chemistry Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Highly Efficient Pd-Catalyzed Cyanation of Aryl Chlorides and Arenesulfonates with Potassium Ferrocyanide in Aqueous Media |
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