Unified Strategy to Access 6H‐Benzofuro[2,3‐b]indoles and 5,6‐Dihydroindolo[2,3‐b]indoles via UV Light‐Mediated Diradical Cyclization
A unified protocol for the construction of 6H‐benzofuro[2,3‐b]indoles and 5,6‐dihydroindolo[2,3‐b]indoles via UV light‐mediated diradical cyclization was developed and preliminary efforts were also made to functionalize at C10b position of 6H‐benzofuro[2,3‐b]indoles. This mild and facile strategy ma...
Gespeichert in:
| Veröffentlicht in: | Advanced synthesis & catalysis 2018-02, Vol.360 (3), p.474-478 |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 478 |
|---|---|
| container_issue | 3 |
| container_start_page | 474 |
| container_title | Advanced synthesis & catalysis |
| container_volume | 360 |
| creator | Cheng, Bin Zu, Bing Li, Yuntong Zhai, Shengxian Xu, Wei Li, Yun Zhai, Hongbin |
| description | A unified protocol for the construction of 6H‐benzofuro[2,3‐b]indoles and 5,6‐dihydroindolo[2,3‐b]indoles via UV light‐mediated diradical cyclization was developed and preliminary efforts were also made to functionalize at C10b position of 6H‐benzofuro[2,3‐b]indoles. This mild and facile strategy may have great potential in the syntheses of natural products and functional materials. |
| doi_str_mv | 10.1002/adsc.201701270 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_wiley</sourceid><recordid>TN_cdi_proquest_journals_1993317403</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1993317403</sourcerecordid><originalsourceid>FETCH-LOGICAL-g2510-64bbef6edd386aaffefbc55e006bafa0b5967e31c2c2492a45b0fbf4c5d644f23</originalsourceid><addsrcrecordid>eNplkL1OwzAUhS0EEqWwMltibYp_YqcZSwoUqYgByoJQ5PindRXiYqegdOIN4Bl5ElKKujDde-75dI90ADjFqI8RIudCBdknCCcIkwTtgQ7mmEUx5un-bmfoEByFsEAtNkiSDvicVtZYreB97UWtZw2sHRxKqUOAfPz98XWhq7UzK--eSI-2uni2lXKlDlBUCrIeb28jO2-Ud7_Gf-7NCjh9hBM7m9etcauVbZMUHFkvlJWihFkjS7sWtXXVMTgwogz65G92wfTq8iEbR5O765tsOIlmhGEU8bgotOFaKTrgQhijTSEZ0wjxQhiBCpbyRFMsiSRxSkTMCmQKE0umeBwbQrvgbPt36d3rSoc6X7iVr9rIHKcppTiJEW2pdEu921I3-dLbF-GbHKN803i-aTzfNZ4PR_fZTtEfeJV9lg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1993317403</pqid></control><display><type>article</type><title>Unified Strategy to Access 6H‐Benzofuro[2,3‐b]indoles and 5,6‐Dihydroindolo[2,3‐b]indoles via UV Light‐Mediated Diradical Cyclization</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Cheng, Bin ; Zu, Bing ; Li, Yuntong ; Zhai, Shengxian ; Xu, Wei ; Li, Yun ; Zhai, Hongbin</creator><creatorcontrib>Cheng, Bin ; Zu, Bing ; Li, Yuntong ; Zhai, Shengxian ; Xu, Wei ; Li, Yun ; Zhai, Hongbin</creatorcontrib><description>A unified protocol for the construction of 6H‐benzofuro[2,3‐b]indoles and 5,6‐dihydroindolo[2,3‐b]indoles via UV light‐mediated diradical cyclization was developed and preliminary efforts were also made to functionalize at C10b position of 6H‐benzofuro[2,3‐b]indoles. This mild and facile strategy may have great potential in the syntheses of natural products and functional materials.</description><identifier>ISSN: 1615-4150</identifier><identifier>EISSN: 1615-4169</identifier><identifier>DOI: 10.1002/adsc.201701270</identifier><language>eng</language><publisher>Heidelberg: Wiley Subscription Services, Inc</publisher><subject>5,6-dihydroindolo[2,3-b]indole ; 6H-benzofuro[2,3-b]indole ; diradical cyclization ; Indoles ; Natural products ; UV light-mediated</subject><ispartof>Advanced synthesis & catalysis, 2018-02, Vol.360 (3), p.474-478</ispartof><rights>2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadsc.201701270$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadsc.201701270$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids></links><search><creatorcontrib>Cheng, Bin</creatorcontrib><creatorcontrib>Zu, Bing</creatorcontrib><creatorcontrib>Li, Yuntong</creatorcontrib><creatorcontrib>Zhai, Shengxian</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Li, Yun</creatorcontrib><creatorcontrib>Zhai, Hongbin</creatorcontrib><title>Unified Strategy to Access 6H‐Benzofuro[2,3‐b]indoles and 5,6‐Dihydroindolo[2,3‐b]indoles via UV Light‐Mediated Diradical Cyclization</title><title>Advanced synthesis & catalysis</title><description>A unified protocol for the construction of 6H‐benzofuro[2,3‐b]indoles and 5,6‐dihydroindolo[2,3‐b]indoles via UV light‐mediated diradical cyclization was developed and preliminary efforts were also made to functionalize at C10b position of 6H‐benzofuro[2,3‐b]indoles. This mild and facile strategy may have great potential in the syntheses of natural products and functional materials.</description><subject>5,6-dihydroindolo[2,3-b]indole</subject><subject>6H-benzofuro[2,3-b]indole</subject><subject>diradical cyclization</subject><subject>Indoles</subject><subject>Natural products</subject><subject>UV light-mediated</subject><issn>1615-4150</issn><issn>1615-4169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNplkL1OwzAUhS0EEqWwMltibYp_YqcZSwoUqYgByoJQ5PindRXiYqegdOIN4Bl5ElKKujDde-75dI90ADjFqI8RIudCBdknCCcIkwTtgQ7mmEUx5un-bmfoEByFsEAtNkiSDvicVtZYreB97UWtZw2sHRxKqUOAfPz98XWhq7UzK--eSI-2uni2lXKlDlBUCrIeb28jO2-Ud7_Gf-7NCjh9hBM7m9etcauVbZMUHFkvlJWihFkjS7sWtXXVMTgwogz65G92wfTq8iEbR5O765tsOIlmhGEU8bgotOFaKTrgQhijTSEZ0wjxQhiBCpbyRFMsiSRxSkTMCmQKE0umeBwbQrvgbPt36d3rSoc6X7iVr9rIHKcppTiJEW2pdEu921I3-dLbF-GbHKN803i-aTzfNZ4PR_fZTtEfeJV9lg</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Cheng, Bin</creator><creator>Zu, Bing</creator><creator>Li, Yuntong</creator><creator>Zhai, Shengxian</creator><creator>Xu, Wei</creator><creator>Li, Yun</creator><creator>Zhai, Hongbin</creator><general>Wiley Subscription Services, Inc</general><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20180201</creationdate><title>Unified Strategy to Access 6H‐Benzofuro[2,3‐b]indoles and 5,6‐Dihydroindolo[2,3‐b]indoles via UV Light‐Mediated Diradical Cyclization</title><author>Cheng, Bin ; Zu, Bing ; Li, Yuntong ; Zhai, Shengxian ; Xu, Wei ; Li, Yun ; Zhai, Hongbin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g2510-64bbef6edd386aaffefbc55e006bafa0b5967e31c2c2492a45b0fbf4c5d644f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>5,6-dihydroindolo[2,3-b]indole</topic><topic>6H-benzofuro[2,3-b]indole</topic><topic>diradical cyclization</topic><topic>Indoles</topic><topic>Natural products</topic><topic>UV light-mediated</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Bin</creatorcontrib><creatorcontrib>Zu, Bing</creatorcontrib><creatorcontrib>Li, Yuntong</creatorcontrib><creatorcontrib>Zhai, Shengxian</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Li, Yun</creatorcontrib><creatorcontrib>Zhai, Hongbin</creatorcontrib><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced synthesis & catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, Bin</au><au>Zu, Bing</au><au>Li, Yuntong</au><au>Zhai, Shengxian</au><au>Xu, Wei</au><au>Li, Yun</au><au>Zhai, Hongbin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unified Strategy to Access 6H‐Benzofuro[2,3‐b]indoles and 5,6‐Dihydroindolo[2,3‐b]indoles via UV Light‐Mediated Diradical Cyclization</atitle><jtitle>Advanced synthesis & catalysis</jtitle><date>2018-02-01</date><risdate>2018</risdate><volume>360</volume><issue>3</issue><spage>474</spage><epage>478</epage><pages>474-478</pages><issn>1615-4150</issn><eissn>1615-4169</eissn><abstract>A unified protocol for the construction of 6H‐benzofuro[2,3‐b]indoles and 5,6‐dihydroindolo[2,3‐b]indoles via UV light‐mediated diradical cyclization was developed and preliminary efforts were also made to functionalize at C10b position of 6H‐benzofuro[2,3‐b]indoles. This mild and facile strategy may have great potential in the syntheses of natural products and functional materials.</abstract><cop>Heidelberg</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adsc.201701270</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1615-4150 |
| ispartof | Advanced synthesis & catalysis, 2018-02, Vol.360 (3), p.474-478 |
| issn | 1615-4150 1615-4169 |
| language | eng |
| recordid | cdi_proquest_journals_1993317403 |
| source | Wiley Online Library Journals Frontfile Complete |
| subjects | 5,6-dihydroindolo[2,3-b]indole 6H-benzofuro[2,3-b]indole diradical cyclization Indoles Natural products UV light-mediated |
| title | Unified Strategy to Access 6H‐Benzofuro[2,3‐b]indoles and 5,6‐Dihydroindolo[2,3‐b]indoles via UV Light‐Mediated Diradical Cyclization |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T01%3A56%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_wiley&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Unified%20Strategy%20to%20Access%206H%E2%80%90Benzofuro%5B2,3%E2%80%90b%5Dindoles%20and%205,6%E2%80%90Dihydroindolo%5B2,3%E2%80%90b%5Dindoles%20via%20UV%20Light%E2%80%90Mediated%20Diradical%20Cyclization&rft.jtitle=Advanced%20synthesis%20&%20catalysis&rft.au=Cheng,%20Bin&rft.date=2018-02-01&rft.volume=360&rft.issue=3&rft.spage=474&rft.epage=478&rft.pages=474-478&rft.issn=1615-4150&rft.eissn=1615-4169&rft_id=info:doi/10.1002/adsc.201701270&rft_dat=%3Cproquest_wiley%3E1993317403%3C/proquest_wiley%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1993317403&rft_id=info:pmid/&rfr_iscdi=true |