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Recent advances in radical-mediated fluorination through C-H and C-C bond cleavage
The C-H and C-C bonds are abundant in organic compounds,yet generally inert in chemical transformations.Therefore,direct functionalization of inert chemical bonds remains challenging.The fluorine-containing compounds are of special interest for their uses in medicinal chemistry.Direct fluorination o...
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Published in: | Science China. Chemistry 2017-02, Vol.60 (2), p.214-222 |
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description | The C-H and C-C bonds are abundant in organic compounds,yet generally inert in chemical transformations.Therefore,direct functionalization of inert chemical bonds remains challenging.The fluorine-containing compounds are of special interest for their uses in medicinal chemistry.Direct fluorination of C-H and C-C bonds undoubtedly represents one of the most ideal and attractive approaches to incorporate fluorine atom into complex molecules.Herein,we summarize the recent advances in radical-mediated C-H and C-C bond fluorination.Three types of transformations are discussed:(1)direct C-H abstraction/fluorination of alkanes;(2)decarboxylative fluorination of alkyl carboxylic acids;(3)ring-opening fluorination. |
doi_str_mv | 10.1007/s11426-016-0399-5 |
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China Chem</addtitle><addtitle>SCIENCE CHINA Chemistry</addtitle><description>The C-H and C-C bonds are abundant in organic compounds,yet generally inert in chemical transformations.Therefore,direct functionalization of inert chemical bonds remains challenging.The fluorine-containing compounds are of special interest for their uses in medicinal chemistry.Direct fluorination of C-H and C-C bonds undoubtedly represents one of the most ideal and attractive approaches to incorporate fluorine atom into complex molecules.Herein,we summarize the recent advances in radical-mediated C-H and C-C bond fluorination.Three types of transformations are discussed:(1)direct C-H abstraction/fluorination of alkanes;(2)decarboxylative fluorination of alkyl carboxylic acids;(3)ring-opening fluorination.</description><subject>Acids</subject><subject>Alkanes</subject><subject>C-C键</subject><subject>Carboxylic acids</subject><subject>Chemical bonds</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Copper</subject><subject>Covalent bonds</subject><subject>Fluorides</subject><subject>Fluorination</subject><subject>Fluorine</subject><subject>Organic compounds</subject><subject>Radicals</subject><subject>Reviews</subject><subject>Ring opening</subject><subject>介导</subject><subject>化学键</subject><subject>含氟化合物</subject><subject>断裂</subject><subject>有机化合物</subject><subject>氟化反应</subject><subject>自由基</subject><issn>1674-7291</issn><issn>1869-1870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9UMFKAzEUDKJgqf0Ab0HP0WSzSTZHWdQKBaHoOWST7HbLNmmTbcG_N7JFbz4Y3hxm3vAGgFuCHwjG4jERUhYcYZJBpUTsAsxIxSUilcCXmXNRIlFIcg0WKW1xHkpxIdgMrNfOOD9CbU_aG5dg72HUtjd6QDtnez06C9vhGGLv9dgHD8dNDMduA2u0hNrbvGvYhEzM4PRJd-4GXLV6SG5x3nPw-fL8US_R6v31rX5aIUNLOiItWleS0jrZNA3LpOKWU25bU-LGSSuobiQjxmZgbiiW2DDLGbdNqZ22dA7up7v7GA5Hl0a1Dcfoc6TKr1acMS5oVpFJZWJIKbpW7WO_0_FLEax-2lNTeyq3p37aUyx7ismTstZ3Lv5d_s90dw7aBN8dsu83iQtCmZBVRb8BvtF9Cw</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Yan, Hong</creator><creator>Zhu, Chen</creator><general>Science China Press</general><general>Springer Nature B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>M2P</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20170201</creationdate><title>Recent advances in radical-mediated fluorination through C-H and C-C bond cleavage</title><author>Yan, Hong ; Zhu, Chen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-a7fe414de9bbb514d86d636dfc40be9d73ab951cd51c06c3090c5d656db4aead3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acids</topic><topic>Alkanes</topic><topic>C-C键</topic><topic>Carboxylic acids</topic><topic>Chemical bonds</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Copper</topic><topic>Covalent bonds</topic><topic>Fluorides</topic><topic>Fluorination</topic><topic>Fluorine</topic><topic>Organic compounds</topic><topic>Radicals</topic><topic>Reviews</topic><topic>Ring opening</topic><topic>介导</topic><topic>化学键</topic><topic>含氟化合物</topic><topic>断裂</topic><topic>有机化合物</topic><topic>氟化反应</topic><topic>自由基</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yan, Hong</creatorcontrib><creatorcontrib>Zhu, Chen</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Science Database</collection><collection>Materials science collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Science China. 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China Chem</stitle><addtitle>SCIENCE CHINA Chemistry</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>60</volume><issue>2</issue><spage>214</spage><epage>222</epage><pages>214-222</pages><issn>1674-7291</issn><eissn>1869-1870</eissn><abstract>The C-H and C-C bonds are abundant in organic compounds,yet generally inert in chemical transformations.Therefore,direct functionalization of inert chemical bonds remains challenging.The fluorine-containing compounds are of special interest for their uses in medicinal chemistry.Direct fluorination of C-H and C-C bonds undoubtedly represents one of the most ideal and attractive approaches to incorporate fluorine atom into complex molecules.Herein,we summarize the recent advances in radical-mediated C-H and C-C bond fluorination.Three types of transformations are discussed:(1)direct C-H abstraction/fluorination of alkanes;(2)decarboxylative fluorination of alkyl carboxylic acids;(3)ring-opening fluorination.</abstract><cop>Beijing</cop><pub>Science China Press</pub><doi>10.1007/s11426-016-0399-5</doi><tpages>9</tpages></addata></record> |
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subjects | Acids Alkanes C-C键 Carboxylic acids Chemical bonds Chemistry Chemistry and Materials Science Chemistry/Food Science Copper Covalent bonds Fluorides Fluorination Fluorine Organic compounds Radicals Reviews Ring opening 介导 化学键 含氟化合物 断裂 有机化合物 氟化反应 自由基 |
title | Recent advances in radical-mediated fluorination through C-H and C-C bond cleavage |
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