KI‐Mediated One‐Pot Transition‐Metal‐Rree Synthesis of 4‐Phenylpyrrolo[1,2‐a]quinoxalines
An efficient and eco‐friendly method for the synthesis of pyrrolo[1,2‐a]quinoxalines is presented. Compared to previous methods, this protocol is transition‐metal‐free and only potassium iodide is required. A series of substituted 4‐phenylpyrrolo[1,2‐a]quinoxalines are obtained in moderate to good y...
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Veröffentlicht in: | European journal of organic chemistry 2020-08, Vol.2020 (31), p.4950-4956 |
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container_title | European journal of organic chemistry |
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creator | Li, Shichen Xie, Caixia Chu, Xianglong Dai, Zhen Feng, Lei Ma, Chen |
description | An efficient and eco‐friendly method for the synthesis of pyrrolo[1,2‐a]quinoxalines is presented. Compared to previous methods, this protocol is transition‐metal‐free and only potassium iodide is required. A series of substituted 4‐phenylpyrrolo[1,2‐a]quinoxalines are obtained in moderate to good yields.
This protocol offered an eco‐friendly and convenient method for the synthesis of pyrrolo[1,2‐a]quinoxalines. In this process, new C=N and C–C bond were formed in mild conditions. A series of pyrrolo[1,2‐a]quinoxaline derivatives were obtained in moderate to good yields. |
doi_str_mv | 10.1002/ejoc.202000791 |
format | Article |
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This protocol offered an eco‐friendly and convenient method for the synthesis of pyrrolo[1,2‐a]quinoxalines. In this process, new C=N and C–C bond were formed in mild conditions. A series of pyrrolo[1,2‐a]quinoxaline derivatives were obtained in moderate to good yields.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.202000791</identifier><language>eng</language><subject>One‐pot ; Pyrrolo[1,2‐a]quinoxalines ; Transition‐metal‐free</subject><ispartof>European journal of organic chemistry, 2020-08, Vol.2020 (31), p.4950-4956</ispartof><rights>2020 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2891-d7a5331e1ac35bce5ad7d8534c94106d87c7a94de02127dc20f36723e1acddd83</citedby><cites>FETCH-LOGICAL-c2891-d7a5331e1ac35bce5ad7d8534c94106d87c7a94de02127dc20f36723e1acddd83</cites><orcidid>0000-0001-8908-4658</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.202000791$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejoc.202000791$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Li, Shichen</creatorcontrib><creatorcontrib>Xie, Caixia</creatorcontrib><creatorcontrib>Chu, Xianglong</creatorcontrib><creatorcontrib>Dai, Zhen</creatorcontrib><creatorcontrib>Feng, Lei</creatorcontrib><creatorcontrib>Ma, Chen</creatorcontrib><title>KI‐Mediated One‐Pot Transition‐Metal‐Rree Synthesis of 4‐Phenylpyrrolo[1,2‐a]quinoxalines</title><title>European journal of organic chemistry</title><description>An efficient and eco‐friendly method for the synthesis of pyrrolo[1,2‐a]quinoxalines is presented. Compared to previous methods, this protocol is transition‐metal‐free and only potassium iodide is required. A series of substituted 4‐phenylpyrrolo[1,2‐a]quinoxalines are obtained in moderate to good yields.
This protocol offered an eco‐friendly and convenient method for the synthesis of pyrrolo[1,2‐a]quinoxalines. In this process, new C=N and C–C bond were formed in mild conditions. A series of pyrrolo[1,2‐a]quinoxaline derivatives were obtained in moderate to good yields.</description><subject>One‐pot</subject><subject>Pyrrolo[1,2‐a]quinoxalines</subject><subject>Transition‐metal‐free</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkE1OwzAUhC0EEqWwZZ0DkPJsJ3G8RFWBQlERFAkJocjYL6qrEIMdBNlxBM7ISUgogiWreT_zzWII2acwogDsEFdOjxgwABCSbpABBSljyCRsdnPCk5hKfrtNdkJYdR6ZZXRA8Hz6-f5xgcaqBk00r7FbL10TLbyqg22sq7__jao6vfKI0XVbN0sMNkSujJLevsS6rZ5a713l7ugB627q_vnF1u5NVbbGsEu2SlUF3PvRIbk5nizGp_FsfjIdH81izXJJYyNUyjlFqjRPHzSmygiTpzzRMqGQmVxooWRiEBhlwmgGJc8E4z1gjMn5kIzWudq7EDyWxZO3j8q3BYWiL6noSyp-S-oAuQZebYXtP-5icjYf_7FfkOZy1Q</recordid><startdate>20200823</startdate><enddate>20200823</enddate><creator>Li, Shichen</creator><creator>Xie, Caixia</creator><creator>Chu, Xianglong</creator><creator>Dai, Zhen</creator><creator>Feng, Lei</creator><creator>Ma, Chen</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-8908-4658</orcidid></search><sort><creationdate>20200823</creationdate><title>KI‐Mediated One‐Pot Transition‐Metal‐Rree Synthesis of 4‐Phenylpyrrolo[1,2‐a]quinoxalines</title><author>Li, Shichen ; Xie, Caixia ; Chu, Xianglong ; Dai, Zhen ; Feng, Lei ; Ma, Chen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2891-d7a5331e1ac35bce5ad7d8534c94106d87c7a94de02127dc20f36723e1acddd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>One‐pot</topic><topic>Pyrrolo[1,2‐a]quinoxalines</topic><topic>Transition‐metal‐free</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Shichen</creatorcontrib><creatorcontrib>Xie, Caixia</creatorcontrib><creatorcontrib>Chu, Xianglong</creatorcontrib><creatorcontrib>Dai, Zhen</creatorcontrib><creatorcontrib>Feng, Lei</creatorcontrib><creatorcontrib>Ma, Chen</creatorcontrib><collection>CrossRef</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Shichen</au><au>Xie, Caixia</au><au>Chu, Xianglong</au><au>Dai, Zhen</au><au>Feng, Lei</au><au>Ma, Chen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>KI‐Mediated One‐Pot Transition‐Metal‐Rree Synthesis of 4‐Phenylpyrrolo[1,2‐a]quinoxalines</atitle><jtitle>European journal of organic chemistry</jtitle><date>2020-08-23</date><risdate>2020</risdate><volume>2020</volume><issue>31</issue><spage>4950</spage><epage>4956</epage><pages>4950-4956</pages><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>An efficient and eco‐friendly method for the synthesis of pyrrolo[1,2‐a]quinoxalines is presented. Compared to previous methods, this protocol is transition‐metal‐free and only potassium iodide is required. A series of substituted 4‐phenylpyrrolo[1,2‐a]quinoxalines are obtained in moderate to good yields.
This protocol offered an eco‐friendly and convenient method for the synthesis of pyrrolo[1,2‐a]quinoxalines. In this process, new C=N and C–C bond were formed in mild conditions. A series of pyrrolo[1,2‐a]quinoxaline derivatives were obtained in moderate to good yields.</abstract><doi>10.1002/ejoc.202000791</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-8908-4658</orcidid></addata></record> |
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subjects | One‐pot Pyrrolo[1,2‐a]quinoxalines Transition‐metal‐free |
title | KI‐Mediated One‐Pot Transition‐Metal‐Rree Synthesis of 4‐Phenylpyrrolo[1,2‐a]quinoxalines |
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