Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes

We describe a copper(I) mediated halogenation via direct C–H functionalization of arenes. The combination of Cu(I)X and (diacetoxyiodo)benzene provides a robust system for halogenation of 2-arylpyridines. High regio- and mono-selectivity was achieved for chlorination, bromination, and iodination of...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Catalysis letters 2018-04, Vol.148 (4), p.1067-1072
Hauptverfasser: Perumgani, Pullaiah C., Parvathaneni, Sai Prathima, Surendra Babu, G. V., Srinivas, K., Mandapati, Mohan Rao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1072
container_issue 4
container_start_page 1067
container_title Catalysis letters
container_volume 148
creator Perumgani, Pullaiah C.
Parvathaneni, Sai Prathima
Surendra Babu, G. V.
Srinivas, K.
Mandapati, Mohan Rao
description We describe a copper(I) mediated halogenation via direct C–H functionalization of arenes. The combination of Cu(I)X and (diacetoxyiodo)benzene provides a robust system for halogenation of 2-arylpyridines. High regio- and mono-selectivity was achieved for chlorination, bromination, and iodination of arene C–H bonds. Graphical Abstract
doi_str_mv 10.1007/s10562-018-2324-5
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2258892718</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A531222797</galeid><sourcerecordid>A531222797</sourcerecordid><originalsourceid>FETCH-LOGICAL-c392t-6d12fd0f234228c5bdf50708d03a27a8cde35ee4ecced09f1dd99621445150c83</originalsourceid><addsrcrecordid>eNp1kE1LAzEQhhdRsFZ_gLcFL3pITWY3zeZY6kcLhYIo9BbWZLKmtJs12Qr-e1NW8CRzmGHmfWaGN8uuGZ0wSsV9ZJRPgVBWESigJPwkGzEugFRCbk5TTRkjhYDNeXYR45ZSKgWTo2w5912H4XZ5ly_qnTOYWx_yF2ycj7hD3bsvzNeh__AkzX2Dbd073-be5g8upDmafBawxXiZndl6F_HqN4-zt6fH1_mCrNbPy_lsRXQhoSdTw8AaaqEoASrN343lVNDK0KIGUVfaYMERS9QaDZWWGSPlFFhZcsapropxdjPs7YL_PGDs1dYfQptOKgBeVRIEO6omg6qpd6hca30fap3C4N5p36J1qT_jBQMAIUUC2ADo4GMMaFUX3L4O34pRdbRYDRarZLE6Wqx4YmBgYtK2DYa_V_6HfgDb7n0m</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2258892718</pqid></control><display><type>article</type><title>Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes</title><source>SpringerLink Journals - AutoHoldings</source><creator>Perumgani, Pullaiah C. ; Parvathaneni, Sai Prathima ; Surendra Babu, G. V. ; Srinivas, K. ; Mandapati, Mohan Rao</creator><creatorcontrib>Perumgani, Pullaiah C. ; Parvathaneni, Sai Prathima ; Surendra Babu, G. V. ; Srinivas, K. ; Mandapati, Mohan Rao</creatorcontrib><description>We describe a copper(I) mediated halogenation via direct C–H functionalization of arenes. The combination of Cu(I)X and (diacetoxyiodo)benzene provides a robust system for halogenation of 2-arylpyridines. High regio- and mono-selectivity was achieved for chlorination, bromination, and iodination of arene C–H bonds. Graphical Abstract</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1007/s10562-018-2324-5</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Aromatic compounds ; Benzene ; Bonds (Securities) ; Bromination ; Catalysis ; Chemistry ; Chemistry and Materials Science ; Copper ; Halogenation ; Industrial Chemistry/Chemical Engineering ; Iodination ; Organometallic Chemistry ; Physical Chemistry ; Selectivity</subject><ispartof>Catalysis letters, 2018-04, Vol.148 (4), p.1067-1072</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Catalysis Letters is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-6d12fd0f234228c5bdf50708d03a27a8cde35ee4ecced09f1dd99621445150c83</citedby><cites>FETCH-LOGICAL-c392t-6d12fd0f234228c5bdf50708d03a27a8cde35ee4ecced09f1dd99621445150c83</cites><orcidid>0000-0002-9605-9802</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10562-018-2324-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10562-018-2324-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids></links><search><creatorcontrib>Perumgani, Pullaiah C.</creatorcontrib><creatorcontrib>Parvathaneni, Sai Prathima</creatorcontrib><creatorcontrib>Surendra Babu, G. V.</creatorcontrib><creatorcontrib>Srinivas, K.</creatorcontrib><creatorcontrib>Mandapati, Mohan Rao</creatorcontrib><title>Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes</title><title>Catalysis letters</title><addtitle>Catal Lett</addtitle><description>We describe a copper(I) mediated halogenation via direct C–H functionalization of arenes. The combination of Cu(I)X and (diacetoxyiodo)benzene provides a robust system for halogenation of 2-arylpyridines. High regio- and mono-selectivity was achieved for chlorination, bromination, and iodination of arene C–H bonds. Graphical Abstract</description><subject>Aromatic compounds</subject><subject>Benzene</subject><subject>Bonds (Securities)</subject><subject>Bromination</subject><subject>Catalysis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Copper</subject><subject>Halogenation</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Iodination</subject><subject>Organometallic Chemistry</subject><subject>Physical Chemistry</subject><subject>Selectivity</subject><issn>1011-372X</issn><issn>1572-879X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kE1LAzEQhhdRsFZ_gLcFL3pITWY3zeZY6kcLhYIo9BbWZLKmtJs12Qr-e1NW8CRzmGHmfWaGN8uuGZ0wSsV9ZJRPgVBWESigJPwkGzEugFRCbk5TTRkjhYDNeXYR45ZSKgWTo2w5912H4XZ5ly_qnTOYWx_yF2ycj7hD3bsvzNeh__AkzX2Dbd073-be5g8upDmafBawxXiZndl6F_HqN4-zt6fH1_mCrNbPy_lsRXQhoSdTw8AaaqEoASrN343lVNDK0KIGUVfaYMERS9QaDZWWGSPlFFhZcsapropxdjPs7YL_PGDs1dYfQptOKgBeVRIEO6omg6qpd6hca30fap3C4N5p36J1qT_jBQMAIUUC2ADo4GMMaFUX3L4O34pRdbRYDRarZLE6Wqx4YmBgYtK2DYa_V_6HfgDb7n0m</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Perumgani, Pullaiah C.</creator><creator>Parvathaneni, Sai Prathima</creator><creator>Surendra Babu, G. V.</creator><creator>Srinivas, K.</creator><creator>Mandapati, Mohan Rao</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-9605-9802</orcidid></search><sort><creationdate>20180401</creationdate><title>Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes</title><author>Perumgani, Pullaiah C. ; Parvathaneni, Sai Prathima ; Surendra Babu, G. V. ; Srinivas, K. ; Mandapati, Mohan Rao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-6d12fd0f234228c5bdf50708d03a27a8cde35ee4ecced09f1dd99621445150c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aromatic compounds</topic><topic>Benzene</topic><topic>Bonds (Securities)</topic><topic>Bromination</topic><topic>Catalysis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Copper</topic><topic>Halogenation</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Iodination</topic><topic>Organometallic Chemistry</topic><topic>Physical Chemistry</topic><topic>Selectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perumgani, Pullaiah C.</creatorcontrib><creatorcontrib>Parvathaneni, Sai Prathima</creatorcontrib><creatorcontrib>Surendra Babu, G. V.</creatorcontrib><creatorcontrib>Srinivas, K.</creatorcontrib><creatorcontrib>Mandapati, Mohan Rao</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; 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 One Academic Eastern Edition (DO NOT USE)</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>Perumgani, Pullaiah C.</au><au>Parvathaneni, Sai Prathima</au><au>Surendra Babu, G. V.</au><au>Srinivas, K.</au><au>Mandapati, Mohan Rao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes</atitle><jtitle>Catalysis letters</jtitle><stitle>Catal Lett</stitle><date>2018-04-01</date><risdate>2018</risdate><volume>148</volume><issue>4</issue><spage>1067</spage><epage>1072</epage><pages>1067-1072</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>We describe a copper(I) mediated halogenation via direct C–H functionalization of arenes. The combination of Cu(I)X and (diacetoxyiodo)benzene provides a robust system for halogenation of 2-arylpyridines. High regio- and mono-selectivity was achieved for chlorination, bromination, and iodination of arene C–H bonds. Graphical Abstract</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10562-018-2324-5</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-9605-9802</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1011-372X
ispartof Catalysis letters, 2018-04, Vol.148 (4), p.1067-1072
issn 1011-372X
1572-879X
language eng
recordid cdi_proquest_journals_2258892718
source SpringerLink Journals - AutoHoldings
subjects Aromatic compounds
Benzene
Bonds (Securities)
Bromination
Catalysis
Chemistry
Chemistry and Materials Science
Copper
Halogenation
Industrial Chemistry/Chemical Engineering
Iodination
Organometallic Chemistry
Physical Chemistry
Selectivity
title Copper(I) Halide for Regioselective Ortho-Halogenation of Directed Arenes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T06%3A15%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Copper(I)%20Halide%20for%20Regioselective%20Ortho-Halogenation%20of%20Directed%20Arenes&rft.jtitle=Catalysis%20letters&rft.au=Perumgani,%20Pullaiah%20C.&rft.date=2018-04-01&rft.volume=148&rft.issue=4&rft.spage=1067&rft.epage=1072&rft.pages=1067-1072&rft.issn=1011-372X&rft.eissn=1572-879X&rft_id=info:doi/10.1007/s10562-018-2324-5&rft_dat=%3Cgale_proqu%3EA531222797%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2258892718&rft_id=info:pmid/&rft_galeid=A531222797&rfr_iscdi=true