A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines
The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[ b ]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-bromophenyl)-1,2,3-thia- and -selenadiazoles wi...
Gespeichert in:
| Veröffentlicht in: | Russian journal of general chemistry 2018-04, Vol.88 (4), p.689-699 |
|---|---|
| Hauptverfasser: | , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 699 |
|---|---|
| container_issue | 4 |
| container_start_page | 689 |
| container_title | Russian journal of general chemistry |
| container_volume | 88 |
| creator | Popova, E. A. Lyapunova, A. G. Petrov, M. L. Panikorovskii, T. L. Androsov, D. A. |
| description | The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[
b
]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-bromophenyl)-1,2,3-thia- and -selenadiazoles with amines in the absence of copper salt, were transformed into 2-aminobenzo[
b
]chalcogenophenes by the action of potassium carbonate and copper(I) iodide in DMF in different yields. |
| doi_str_mv | 10.1134/S1070363218040126 |
| format | Article |
| fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2052869453</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A726585839</galeid><sourcerecordid>A726585839</sourcerecordid><originalsourceid>FETCH-LOGICAL-c355t-261aec18d9f3e2bfd434639d3ae0bb243929d2475b440a5fca3d44bc208bec9e3</originalsourceid><addsrcrecordid>eNp1kd9qFDEUxgdRsFYfwLuANwpNzd_ZmcvpYlUoKLS9EhnOJCe7KTPJmEyF3efqA5rtCr0QyUXC-b7fdw45VfWWs3POpfp4zdmKyVoK3jDFuKifVSe8Zg2VUrPn5V1ketBfVq9yvmOMM1aLk-qhI-sYfmPwGBbSzXOKYLZkiUTQbvIhDhj28cfw02xhNHGDIc5bDJjJBWS0JIbCzzMmuoYFxt2-1G4ShOximmDxRY-OKPpe0IsUp0d4N36g_EycSfoUaj3s41hifSDLFsn3hBmDwQMNj70IBEsOI2F-Xb1wMGZ88_c-rW4vP92sv9Crb5-_rrsraqTWCxU1BzS8sa2TKAZnlVS1bK0EZMMglGxFa4Va6UEpBtoZkFapwQjWDGhalKfVu2Nu-ZVf95iX_i7ep1Ba9oJp0dSt0rK4zo-uDYzY--DiksCUY3HyJgZ0vtS7lah1oxvZFoAfAZNizgldPyc_Qdr1nPWHbfb_bLMw4sjk4g0bTE-j_B_6A9ONoeY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2052869453</pqid></control><display><type>article</type><title>A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines</title><source>SpringerLink Journals - AutoHoldings</source><creator>Popova, E. A. ; Lyapunova, A. G. ; Petrov, M. L. ; Panikorovskii, T. L. ; Androsov, D. A.</creator><creatorcontrib>Popova, E. A. ; Lyapunova, A. G. ; Petrov, M. L. ; Panikorovskii, T. L. ; Androsov, D. A.</creatorcontrib><description>The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[
b
]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-bromophenyl)-1,2,3-thia- and -selenadiazoles with amines in the absence of copper salt, were transformed into 2-aminobenzo[
b
]chalcogenophenes by the action of potassium carbonate and copper(I) iodide in DMF in different yields.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363218040126</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Amines ; Aromatic compounds ; Carbonates ; Chemical industry ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Copper ; Cuprous iodide ; Field-effect transistors ; Potash ; Potassium ; Potassium carbonate ; Thiophene</subject><ispartof>Russian journal of general chemistry, 2018-04, Vol.88 (4), p.689-699</ispartof><rights>Pleiades Publishing, Ltd. 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Copyright Springer Science & Business Media 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c355t-261aec18d9f3e2bfd434639d3ae0bb243929d2475b440a5fca3d44bc208bec9e3</citedby><cites>FETCH-LOGICAL-c355t-261aec18d9f3e2bfd434639d3ae0bb243929d2475b440a5fca3d44bc208bec9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363218040126$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363218040126$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Popova, E. A.</creatorcontrib><creatorcontrib>Lyapunova, A. G.</creatorcontrib><creatorcontrib>Petrov, M. L.</creatorcontrib><creatorcontrib>Panikorovskii, T. L.</creatorcontrib><creatorcontrib>Androsov, D. A.</creatorcontrib><title>A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[
b
]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-bromophenyl)-1,2,3-thia- and -selenadiazoles with amines in the absence of copper salt, were transformed into 2-aminobenzo[
b
]chalcogenophenes by the action of potassium carbonate and copper(I) iodide in DMF in different yields.</description><subject>Amines</subject><subject>Aromatic compounds</subject><subject>Carbonates</subject><subject>Chemical industry</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Copper</subject><subject>Cuprous iodide</subject><subject>Field-effect transistors</subject><subject>Potash</subject><subject>Potassium</subject><subject>Potassium carbonate</subject><subject>Thiophene</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kd9qFDEUxgdRsFYfwLuANwpNzd_ZmcvpYlUoKLS9EhnOJCe7KTPJmEyF3efqA5rtCr0QyUXC-b7fdw45VfWWs3POpfp4zdmKyVoK3jDFuKifVSe8Zg2VUrPn5V1ketBfVq9yvmOMM1aLk-qhI-sYfmPwGBbSzXOKYLZkiUTQbvIhDhj28cfw02xhNHGDIc5bDJjJBWS0JIbCzzMmuoYFxt2-1G4ShOximmDxRY-OKPpe0IsUp0d4N36g_EycSfoUaj3s41hifSDLFsn3hBmDwQMNj70IBEsOI2F-Xb1wMGZ88_c-rW4vP92sv9Crb5-_rrsraqTWCxU1BzS8sa2TKAZnlVS1bK0EZMMglGxFa4Va6UEpBtoZkFapwQjWDGhalKfVu2Nu-ZVf95iX_i7ep1Ba9oJp0dSt0rK4zo-uDYzY--DiksCUY3HyJgZ0vtS7lah1oxvZFoAfAZNizgldPyc_Qdr1nPWHbfb_bLMw4sjk4g0bTE-j_B_6A9ONoeY</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Popova, E. A.</creator><creator>Lyapunova, A. G.</creator><creator>Petrov, M. L.</creator><creator>Panikorovskii, T. L.</creator><creator>Androsov, D. A.</creator><general>Pleiades Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20180401</creationdate><title>A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines</title><author>Popova, E. A. ; Lyapunova, A. G. ; Petrov, M. L. ; Panikorovskii, T. L. ; Androsov, D. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-261aec18d9f3e2bfd434639d3ae0bb243929d2475b440a5fca3d44bc208bec9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amines</topic><topic>Aromatic compounds</topic><topic>Carbonates</topic><topic>Chemical industry</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Copper</topic><topic>Cuprous iodide</topic><topic>Field-effect transistors</topic><topic>Potash</topic><topic>Potassium</topic><topic>Potassium carbonate</topic><topic>Thiophene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Popova, E. A.</creatorcontrib><creatorcontrib>Lyapunova, A. G.</creatorcontrib><creatorcontrib>Petrov, M. L.</creatorcontrib><creatorcontrib>Panikorovskii, T. L.</creatorcontrib><creatorcontrib>Androsov, D. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Popova, E. A.</au><au>Lyapunova, A. G.</au><au>Petrov, M. L.</au><au>Panikorovskii, T. L.</au><au>Androsov, D. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2018-04-01</date><risdate>2018</risdate><volume>88</volume><issue>4</issue><spage>689</spage><epage>699</epage><pages>689-699</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[
b
]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-bromophenyl)-1,2,3-thia- and -selenadiazoles with amines in the absence of copper salt, were transformed into 2-aminobenzo[
b
]chalcogenophenes by the action of potassium carbonate and copper(I) iodide in DMF in different yields.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363218040126</doi><tpages>11</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1070-3632 |
| ispartof | Russian journal of general chemistry, 2018-04, Vol.88 (4), p.689-699 |
| issn | 1070-3632 1608-3350 |
| language | eng |
| recordid | cdi_proquest_journals_2052869453 |
| source | SpringerLink Journals - AutoHoldings |
| subjects | Amines Aromatic compounds Carbonates Chemical industry Chemistry Chemistry and Materials Science Chemistry/Food Science Copper Cuprous iodide Field-effect transistors Potash Potassium Potassium carbonate Thiophene |
| title | A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A58%3A09IST&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=A%20Convenient%20Approach%20to%202-Aminobenzo%5Bb%5Dchalcogenophenes%20Based%20on%20Copper-Catalyzed%20Transformation%20of%204-(2-Bromophenyl)-1,2,3-chalcogenodiazoles%20in%20the%20Presence%20of%20a%20Base%20and%20Amines&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Popova,%20E.%20A.&rft.date=2018-04-01&rft.volume=88&rft.issue=4&rft.spage=689&rft.epage=699&rft.pages=689-699&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363218040126&rft_dat=%3Cgale_proqu%3EA726585839%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=2052869453&rft_id=info:pmid/&rft_galeid=A726585839&rfr_iscdi=true |