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Visible‐Light‐Driven Base‐Promoted Radical Cascade Difluoroalkylation‐Cyclization‐Iodination of 1,6‐Enynes with Ethyl Difluoroiodoacetate
A visible‐light‐driven base‐promoted radical cascade difluoroalkylation/5‐exo‐dig cyclization/iodination of 1,6‐enynes with ethyl difluoroiodoacetate was developed under catalyst‐free and oxidant‐free conditions. The difluoroalkylated pyrrolidines and tetrahydrofuran derivatives were generated with...
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Published in: | European journal of organic chemistry 2022-02, Vol.2022 (5), p.n/a |
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container_title | European journal of organic chemistry |
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creator | Wang, Yan Liu, Ruyan Zhou, Pengsheng Wu, Jianglong Li, Wenshuang Wang, Chenyu Li, Hao Li, Dianjun Yang, Jinhui |
description | A visible‐light‐driven base‐promoted radical cascade difluoroalkylation/5‐exo‐dig cyclization/iodination of 1,6‐enynes with ethyl difluoroiodoacetate was developed under catalyst‐free and oxidant‐free conditions. The difluoroalkylated pyrrolidines and tetrahydrofuran derivatives were generated with good functional group tolerance and high Z/E stereoselectivity. This reaction provided an alternative and mild method for the preparation of highly functionalized and vinyl C−I bonds containing five‐membered heterocyclic products.
A visible‐light‐driven base‐enabled free radical reaction of 1,6‐enynes and ICF2COOEt was developed via cascade difluoroalkylation/5‐exo‐dig cyclization/iodination without catalyst and oxidants. The reaction provided difluoroalkylated and vinyl C−I bonds containing pyrrolidines and tetrahydrofuran derivatives in good yields and excellent Z/E stereoselectivity. |
doi_str_mv | 10.1002/ejoc.202101395 |
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A visible‐light‐driven base‐enabled free radical reaction of 1,6‐enynes and ICF2COOEt was developed via cascade difluoroalkylation/5‐exo‐dig cyclization/iodination without catalyst and oxidants. The reaction provided difluoroalkylated and vinyl C−I bonds containing pyrrolidines and tetrahydrofuran derivatives in good yields and excellent Z/E stereoselectivity.</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.202101395</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Base-promoted ; Cyclization ; Difluoroalkylation ; Functional groups ; Iodination ; Oxidizing agents ; Radical reactions ; Stereoselectivity ; Tetrahydrofuran ; Visible-light-driven</subject><ispartof>European journal of organic chemistry, 2022-02, Vol.2022 (5), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3175-3e1f529044efae0c9a85afd42915d22f1ced3a89a12d7496e9cf0dc3d67d33663</citedby><cites>FETCH-LOGICAL-c3175-3e1f529044efae0c9a85afd42915d22f1ced3a89a12d7496e9cf0dc3d67d33663</cites><orcidid>0000-0002-9381-1560 ; 0000-0002-2353-641X ; 0000-0002-3980-7886</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Liu, Ruyan</creatorcontrib><creatorcontrib>Zhou, Pengsheng</creatorcontrib><creatorcontrib>Wu, Jianglong</creatorcontrib><creatorcontrib>Li, Wenshuang</creatorcontrib><creatorcontrib>Wang, Chenyu</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Li, Dianjun</creatorcontrib><creatorcontrib>Yang, Jinhui</creatorcontrib><title>Visible‐Light‐Driven Base‐Promoted Radical Cascade Difluoroalkylation‐Cyclization‐Iodination of 1,6‐Enynes with Ethyl Difluoroiodoacetate</title><title>European journal of organic chemistry</title><description>A visible‐light‐driven base‐promoted radical cascade difluoroalkylation/5‐exo‐dig cyclization/iodination of 1,6‐enynes with ethyl difluoroiodoacetate was developed under catalyst‐free and oxidant‐free conditions. The difluoroalkylated pyrrolidines and tetrahydrofuran derivatives were generated with good functional group tolerance and high Z/E stereoselectivity. This reaction provided an alternative and mild method for the preparation of highly functionalized and vinyl C−I bonds containing five‐membered heterocyclic products.
A visible‐light‐driven base‐enabled free radical reaction of 1,6‐enynes and ICF2COOEt was developed via cascade difluoroalkylation/5‐exo‐dig cyclization/iodination without catalyst and oxidants. The reaction provided difluoroalkylated and vinyl C−I bonds containing pyrrolidines and tetrahydrofuran derivatives in good yields and excellent Z/E stereoselectivity.</description><subject>Base-promoted</subject><subject>Cyclization</subject><subject>Difluoroalkylation</subject><subject>Functional groups</subject><subject>Iodination</subject><subject>Oxidizing agents</subject><subject>Radical reactions</subject><subject>Stereoselectivity</subject><subject>Tetrahydrofuran</subject><subject>Visible-light-driven</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFUMtOwzAQjBBIPK-cI3ElZW0nLj5CKC9VAiFA3CJjr6mLicFOqcKJT-DCD_IlpJTHkdPsjGZmpUmSTQI9AkB3cOxVjwIlQJgoFpIVAkJkwAUsdnfO8owIdrOcrMY4BgDBOVlJ3q9ttLcOP17fhvZu1HR4EOwz1um-jDP1PPgH36BOL6S2Srq0lFFJjemBNW7ig5fuvnWysb7u3GWrnH35YSde2_qLpN6kZJt32qBua4zp1DajdNCMWvdbZL32UmEjG1xPlox0ETe-cS25OhxclsfZ8OzopNwbZoqRfpExJKagAvIcjURQQu4W0uicClJoSg1RqJncFZJQ3c8FR6EMaMU072vGOGdryda89zH4pwnGphr7Sai7lxXltKAMoM86V2_uUsHHGNBUj8E-yNBWBKrZ9NVs-up3-i4g5oGpddj-464Gp2flX_YTN5KRLA</recordid><startdate>20220204</startdate><enddate>20220204</enddate><creator>Wang, Yan</creator><creator>Liu, Ruyan</creator><creator>Zhou, Pengsheng</creator><creator>Wu, Jianglong</creator><creator>Li, Wenshuang</creator><creator>Wang, Chenyu</creator><creator>Li, Hao</creator><creator>Li, Dianjun</creator><creator>Yang, Jinhui</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-9381-1560</orcidid><orcidid>https://orcid.org/0000-0002-2353-641X</orcidid><orcidid>https://orcid.org/0000-0002-3980-7886</orcidid></search><sort><creationdate>20220204</creationdate><title>Visible‐Light‐Driven Base‐Promoted Radical Cascade Difluoroalkylation‐Cyclization‐Iodination of 1,6‐Enynes with Ethyl Difluoroiodoacetate</title><author>Wang, Yan ; Liu, Ruyan ; Zhou, Pengsheng ; Wu, Jianglong ; Li, Wenshuang ; Wang, Chenyu ; Li, Hao ; Li, Dianjun ; Yang, Jinhui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3175-3e1f529044efae0c9a85afd42915d22f1ced3a89a12d7496e9cf0dc3d67d33663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Base-promoted</topic><topic>Cyclization</topic><topic>Difluoroalkylation</topic><topic>Functional groups</topic><topic>Iodination</topic><topic>Oxidizing agents</topic><topic>Radical reactions</topic><topic>Stereoselectivity</topic><topic>Tetrahydrofuran</topic><topic>Visible-light-driven</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Liu, Ruyan</creatorcontrib><creatorcontrib>Zhou, Pengsheng</creatorcontrib><creatorcontrib>Wu, Jianglong</creatorcontrib><creatorcontrib>Li, Wenshuang</creatorcontrib><creatorcontrib>Wang, Chenyu</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Li, Dianjun</creatorcontrib><creatorcontrib>Yang, Jinhui</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, Yan</au><au>Liu, Ruyan</au><au>Zhou, Pengsheng</au><au>Wu, Jianglong</au><au>Li, Wenshuang</au><au>Wang, Chenyu</au><au>Li, Hao</au><au>Li, Dianjun</au><au>Yang, Jinhui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visible‐Light‐Driven Base‐Promoted Radical Cascade Difluoroalkylation‐Cyclization‐Iodination of 1,6‐Enynes with Ethyl Difluoroiodoacetate</atitle><jtitle>European journal of organic chemistry</jtitle><date>2022-02-04</date><risdate>2022</risdate><volume>2022</volume><issue>5</issue><epage>n/a</epage><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>A visible‐light‐driven base‐promoted radical cascade difluoroalkylation/5‐exo‐dig cyclization/iodination of 1,6‐enynes with ethyl difluoroiodoacetate was developed under catalyst‐free and oxidant‐free conditions. The difluoroalkylated pyrrolidines and tetrahydrofuran derivatives were generated with good functional group tolerance and high Z/E stereoselectivity. This reaction provided an alternative and mild method for the preparation of highly functionalized and vinyl C−I bonds containing five‐membered heterocyclic products.
A visible‐light‐driven base‐enabled free radical reaction of 1,6‐enynes and ICF2COOEt was developed via cascade difluoroalkylation/5‐exo‐dig cyclization/iodination without catalyst and oxidants. The reaction provided difluoroalkylated and vinyl C−I bonds containing pyrrolidines and tetrahydrofuran derivatives in good yields and excellent Z/E stereoselectivity.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ejoc.202101395</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-9381-1560</orcidid><orcidid>https://orcid.org/0000-0002-2353-641X</orcidid><orcidid>https://orcid.org/0000-0002-3980-7886</orcidid></addata></record> |
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subjects | Base-promoted Cyclization Difluoroalkylation Functional groups Iodination Oxidizing agents Radical reactions Stereoselectivity Tetrahydrofuran Visible-light-driven |
title | Visible‐Light‐Driven Base‐Promoted Radical Cascade Difluoroalkylation‐Cyclization‐Iodination of 1,6‐Enynes with Ethyl Difluoroiodoacetate |
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