Synthesis of Hexahydrospiroquinoline‐4,1′‐pyrroloquinoline‐2′,5(1H,4′H)‐diones] from 5,6‐dihydro‐4H‐pyrroloquinoline‐1,2‐dione Using Fe3O4@Cu(OH)x as a Nanocatalyst
The tricyclic isatin, 5,6‐dihydro‐4H‐pyrrolo[3,2,1‐ij]quinoline‐1,2‐dione, undergoes three‐component, one‐pot reactions with 1‐aryl‐3‐methylpyrazole‐5‐amines and cyclohexane‐1,3‐diones producing hexacyclic spiro products, hexahydrospiro[pyrazolo[3,4‐b]quinoline‐4,1‐pyrrolo[3,2,1‐ij]quinoline‐2′,5(1H...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2019-07, Vol.56 (7), p.1999-2007 |
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container_end_page | 2007 |
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container_issue | 7 |
container_start_page | 1999 |
container_title | Journal of heterocyclic chemistry |
container_volume | 56 |
creator | Baradarani, Mehdi M Bahman Ebrahimi Saatluo Ghabeli, Shiva Shokri, Zahra Shahbazi, Masoumeh Joule, John A |
description | The tricyclic isatin, 5,6‐dihydro‐4H‐pyrrolo[3,2,1‐ij]quinoline‐1,2‐dione, undergoes three‐component, one‐pot reactions with 1‐aryl‐3‐methylpyrazole‐5‐amines and cyclohexane‐1,3‐diones producing hexacyclic spiro products, hexahydrospiro[pyrazolo[3,4‐b]quinoline‐4,1‐pyrrolo[3,2,1‐ij]quinoline‐2′,5(1H,4′H)‐diones]. Comparable spiro condensation products are also obtained using 4‐hydroxy‐2H‐1‐benzopyran‐2‐one in place of cyclohexane‐1,3‐diones. |
doi_str_mv | 10.1002/jhet.3579 |
format | Article |
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Comparable spiro condensation products are also obtained using 4‐hydroxy‐2H‐1‐benzopyran‐2‐one in place of cyclohexane‐1,3‐diones.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.3579</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Amines ; Aromatic compounds ; Condensates ; Cyclohexane ; Iron oxides ; Quinoline</subject><ispartof>Journal of heterocyclic chemistry, 2019-07, Vol.56 (7), p.1999-2007</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Baradarani, Mehdi M</creatorcontrib><creatorcontrib>Bahman Ebrahimi Saatluo</creatorcontrib><creatorcontrib>Ghabeli, Shiva</creatorcontrib><creatorcontrib>Shokri, Zahra</creatorcontrib><creatorcontrib>Shahbazi, Masoumeh</creatorcontrib><creatorcontrib>Joule, John A</creatorcontrib><title>Synthesis of Hexahydrospiroquinoline‐4,1′‐pyrroloquinoline‐2′,5(1H,4′H)‐diones] from 5,6‐dihydro‐4H‐pyrroloquinoline‐1,2‐dione Using Fe3O4@Cu(OH)x as a Nanocatalyst</title><title>Journal of heterocyclic chemistry</title><description>The tricyclic isatin, 5,6‐dihydro‐4H‐pyrrolo[3,2,1‐ij]quinoline‐1,2‐dione, undergoes three‐component, one‐pot reactions with 1‐aryl‐3‐methylpyrazole‐5‐amines and cyclohexane‐1,3‐diones producing hexacyclic spiro products, hexahydrospiro[pyrazolo[3,4‐b]quinoline‐4,1‐pyrrolo[3,2,1‐ij]quinoline‐2′,5(1H,4′H)‐diones]. Comparable spiro condensation products are also obtained using 4‐hydroxy‐2H‐1‐benzopyran‐2‐one in place of cyclohexane‐1,3‐diones.</description><subject>Amines</subject><subject>Aromatic compounds</subject><subject>Condensates</subject><subject>Cyclohexane</subject><subject>Iron oxides</subject><subject>Quinoline</subject><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBA0NNAzNDAw0s_KSC3RMzY1t2Ri4DS0NDHWNTW0NGZh4ATKGekamhpFcDBwFRdnAbmGxubmnAx7givzSjJSizOLFfLTFDxSKxIzKlOK8osLMovyC0sz8_JzMvNSHzVMMNExfNSwCcgoqCwqys9BkTMCyuiYahh66JgAWR6aQKGUzPy81OJYhbSi_FwFUx0zsBDYZJBZHtjNMdQxgmlVCC3OzEtXcEs19jdxcC7V8PfQrFBILFZIVPBLzMtPTixJzKksLuFhYE1LzClO5YXS3AzKbq4hzh66BSDHpxaXxGfllxblAaXijYxMgcjA3MLAmDhVACtEddM</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Baradarani, Mehdi M</creator><creator>Bahman Ebrahimi Saatluo</creator><creator>Ghabeli, Shiva</creator><creator>Shokri, Zahra</creator><creator>Shahbazi, Masoumeh</creator><creator>Joule, John A</creator><general>Wiley Subscription Services, Inc</general><scope/></search><sort><creationdate>20190701</creationdate><title>Synthesis of Hexahydrospiroquinoline‐4,1′‐pyrroloquinoline‐2′,5(1H,4′H)‐diones] from 5,6‐dihydro‐4H‐pyrroloquinoline‐1,2‐dione Using Fe3O4@Cu(OH)x as a Nanocatalyst</title><author>Baradarani, Mehdi M ; Bahman Ebrahimi Saatluo ; Ghabeli, Shiva ; Shokri, Zahra ; Shahbazi, Masoumeh ; Joule, John A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_22522507803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Amines</topic><topic>Aromatic compounds</topic><topic>Condensates</topic><topic>Cyclohexane</topic><topic>Iron oxides</topic><topic>Quinoline</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baradarani, Mehdi M</creatorcontrib><creatorcontrib>Bahman Ebrahimi Saatluo</creatorcontrib><creatorcontrib>Ghabeli, Shiva</creatorcontrib><creatorcontrib>Shokri, Zahra</creatorcontrib><creatorcontrib>Shahbazi, Masoumeh</creatorcontrib><creatorcontrib>Joule, John A</creatorcontrib><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baradarani, Mehdi M</au><au>Bahman Ebrahimi Saatluo</au><au>Ghabeli, Shiva</au><au>Shokri, Zahra</au><au>Shahbazi, Masoumeh</au><au>Joule, John A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Hexahydrospiroquinoline‐4,1′‐pyrroloquinoline‐2′,5(1H,4′H)‐diones] from 5,6‐dihydro‐4H‐pyrroloquinoline‐1,2‐dione Using Fe3O4@Cu(OH)x as a Nanocatalyst</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2019-07-01</date><risdate>2019</risdate><volume>56</volume><issue>7</issue><spage>1999</spage><epage>2007</epage><pages>1999-2007</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>The tricyclic isatin, 5,6‐dihydro‐4H‐pyrrolo[3,2,1‐ij]quinoline‐1,2‐dione, undergoes three‐component, one‐pot reactions with 1‐aryl‐3‐methylpyrazole‐5‐amines and cyclohexane‐1,3‐diones producing hexacyclic spiro products, hexahydrospiro[pyrazolo[3,4‐b]quinoline‐4,1‐pyrrolo[3,2,1‐ij]quinoline‐2′,5(1H,4′H)‐diones]. Comparable spiro condensation products are also obtained using 4‐hydroxy‐2H‐1‐benzopyran‐2‐one in place of cyclohexane‐1,3‐diones.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jhet.3579</doi></addata></record> |
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source | Wiley-Blackwell Journals |
subjects | Amines Aromatic compounds Condensates Cyclohexane Iron oxides Quinoline |
title | Synthesis of Hexahydrospiroquinoline‐4,1′‐pyrroloquinoline‐2′,5(1H,4′H)‐diones] from 5,6‐dihydro‐4H‐pyrroloquinoline‐1,2‐dione Using Fe3O4@Cu(OH)x as a Nanocatalyst |
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