Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1H)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions
A photo‐induced direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, and gram‐scale synthesis. A photo‐promoted direc...
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| Veröffentlicht in: | European journal of organic chemistry 2023-04, Vol.26 (13), p.n/a |
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| container_title | European journal of organic chemistry |
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| creator | Wang, Bin Feng, Yun Zhang, Yuepan Wang, Shoucai Zhou, Xinlei Chen, Ziren Xia, Yu Jin, Weiwei Iqbal, Azhar Liu, Chenjiang Zhang, Yonghong |
| description | A photo‐induced direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, and gram‐scale synthesis.
A photo‐promoted direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, gram‐scale synthesis, and catalyst‐free conditions. |
| doi_str_mv | 10.1002/ejoc.202300044 |
| format | Article |
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A photo‐promoted direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, gram‐scale synthesis, and catalyst‐free conditions.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.202300044</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>arylation ; aryltriazenes ; Catalysts ; Functional groups ; metal-free ; photocatalysis ; quinoxalin-2(1H)-ones</subject><ispartof>European journal of organic chemistry, 2023-04, Vol.26 (13), p.n/a</ispartof><rights>2023 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3174-615104037e2c30ded2ede85ba7752e3bd4e788c302e76562c9d790092cdc87553</citedby><cites>FETCH-LOGICAL-c3174-615104037e2c30ded2ede85ba7752e3bd4e788c302e76562c9d790092cdc87553</cites><orcidid>0000-0002-7740-9408</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fejoc.202300044$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejoc.202300044$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Feng, Yun</creatorcontrib><creatorcontrib>Zhang, Yuepan</creatorcontrib><creatorcontrib>Wang, Shoucai</creatorcontrib><creatorcontrib>Zhou, Xinlei</creatorcontrib><creatorcontrib>Chen, Ziren</creatorcontrib><creatorcontrib>Xia, Yu</creatorcontrib><creatorcontrib>Jin, Weiwei</creatorcontrib><creatorcontrib>Iqbal, Azhar</creatorcontrib><creatorcontrib>Liu, Chenjiang</creatorcontrib><creatorcontrib>Zhang, Yonghong</creatorcontrib><title>Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1H)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions</title><title>European journal of organic chemistry</title><description>A photo‐induced direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, and gram‐scale synthesis.
A photo‐promoted direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, gram‐scale synthesis, and catalyst‐free conditions.</description><subject>arylation</subject><subject>aryltriazenes</subject><subject>Catalysts</subject><subject>Functional groups</subject><subject>metal-free</subject><subject>photocatalysis</subject><subject>quinoxalin-2(1H)-ones</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LAzEQhhdR8PPqOeBFD1vztZvmWNZqlUIVFLwt6WaKKdukJltrPYknj-JP7C8xtaJHTzPMPO-8zJskhwS3CMb0FMaualFMGcaY841kh2ApU5xLvBl7znhKJLvfTnZDGEdE5jnZSd6uH1zjlq8fZ948gUVnxkPVoGL5_tlDHb-oVWOcRW6EbmbGumdVGxtpekx6J7EOLAQ0N83DN9t4o15gNZpZDR4VqlH1IjQRPPcASFmNOpOhARsdnNVmdTvsJ1sjVQc4-Kl7yd1597bopf3BxWXR6acVI4KnOckI5pgJoBXDGjQFDe1sqITIKLCh5iDa7biiIPIsp5XUQsY3aaWrtsgytpccre9OvXucQWjKsZt5Gy1LKiSTmHAuI9VaU5V3IXgYlVNvJsovSoLLVc7lKufyN-cokGvB3NSw-Icuu1eD4k_7BS31hos</recordid><startdate>20230403</startdate><enddate>20230403</enddate><creator>Wang, Bin</creator><creator>Feng, Yun</creator><creator>Zhang, Yuepan</creator><creator>Wang, Shoucai</creator><creator>Zhou, Xinlei</creator><creator>Chen, Ziren</creator><creator>Xia, Yu</creator><creator>Jin, Weiwei</creator><creator>Iqbal, Azhar</creator><creator>Liu, Chenjiang</creator><creator>Zhang, Yonghong</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-7740-9408</orcidid></search><sort><creationdate>20230403</creationdate><title>Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1H)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions</title><author>Wang, Bin ; Feng, Yun ; Zhang, Yuepan ; Wang, Shoucai ; Zhou, Xinlei ; Chen, Ziren ; Xia, Yu ; Jin, Weiwei ; Iqbal, Azhar ; Liu, Chenjiang ; Zhang, Yonghong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3174-615104037e2c30ded2ede85ba7752e3bd4e788c302e76562c9d790092cdc87553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>arylation</topic><topic>aryltriazenes</topic><topic>Catalysts</topic><topic>Functional groups</topic><topic>metal-free</topic><topic>photocatalysis</topic><topic>quinoxalin-2(1H)-ones</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Feng, Yun</creatorcontrib><creatorcontrib>Zhang, Yuepan</creatorcontrib><creatorcontrib>Wang, Shoucai</creatorcontrib><creatorcontrib>Zhou, Xinlei</creatorcontrib><creatorcontrib>Chen, Ziren</creatorcontrib><creatorcontrib>Xia, Yu</creatorcontrib><creatorcontrib>Jin, Weiwei</creatorcontrib><creatorcontrib>Iqbal, Azhar</creatorcontrib><creatorcontrib>Liu, Chenjiang</creatorcontrib><creatorcontrib>Zhang, Yonghong</creatorcontrib><collection>CrossRef</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Bin</au><au>Feng, Yun</au><au>Zhang, Yuepan</au><au>Wang, Shoucai</au><au>Zhou, Xinlei</au><au>Chen, Ziren</au><au>Xia, Yu</au><au>Jin, Weiwei</au><au>Iqbal, Azhar</au><au>Liu, Chenjiang</au><au>Zhang, Yonghong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1H)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions</atitle><jtitle>European journal of organic chemistry</jtitle><date>2023-04-03</date><risdate>2023</risdate><volume>26</volume><issue>13</issue><epage>n/a</epage><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>A photo‐induced direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, and gram‐scale synthesis.
A photo‐promoted direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, gram‐scale synthesis, and catalyst‐free conditions.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ejoc.202300044</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-7740-9408</orcidid></addata></record> |
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| subjects | arylation aryltriazenes Catalysts Functional groups metal-free photocatalysis quinoxalin-2(1H)-ones |
| title | Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1H)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions |
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