Progress in Copper-Mediated Formation of Trifluoromethylated Arenes
Development of transition‐metal‐catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few years. Among the many methods developed, copper‐mediated trifluororomethylation has made significant progress and is the subject of this min...
Saved in:
| Published in | European journal of organic chemistry Vol. 2012; no. 34; pp. 6679 - 6687 |
|---|---|
| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
01.12.2012
WILEY‐VCH Verlag Wiley-VCH Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Development of transition‐metal‐catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few years. Among the many methods developed, copper‐mediated trifluororomethylation has made significant progress and is the subject of this minireview.
Recent advances in copper‐mediated trifluoromethylation of arene substrates are reviewed. |
|---|---|
| AbstractList | Development of transition‐metal‐catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few years. Among the many methods developed, copper‐mediated trifluororomethylation has made significant progress and is the subject of this minireview.
Recent advances in copper‐mediated trifluoromethylation of arene substrates are reviewed. Development of transition-metal-catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few years. Among the many methods developed, copper-mediated trifluororomethylation has made significant progress and is the subject of this minireview. [PUBLICATION ABSTRACT] Development of transition‐metal‐catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few years. Among the many methods developed, copper‐mediated trifluororomethylation has made significant progress and is the subject of this minireview. |
| Author | Shen, Qilong Liu, Tianfei |
| Author_xml | – sequence: 1 givenname: Tianfei surname: Liu fullname: Liu, Tianfei organization: Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. China, http://sourcedb.cas.cn/sourcedb_sioc_cas/en/expert/201005/t20100521_2852566.html – sequence: 2 givenname: Qilong surname: Shen fullname: Shen, Qilong email: shenql@sioc.ac.cn organization: Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. China, http://sourcedb.cas.cn/sourcedb_sioc_cas/en/expert/201005/t20100521_2852566.html |
| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26735916$$DView record in Pascal Francis |
| BookMark | eNqFkE1PGzEQhq0KpPJ17XmlqscNM96NvT7SFeFDAaICourFcnbHrdPNOtgbQf49C4kihFT1NHN4nnk17z7baX1LjH1BGCAAP6aZrwYckAOIvPjE9hCUSkEo2On3PMtTVNnPz2w_xhkAKCFwj5WT4H8HijFxbVL6xYJCekW1Mx3VyciHuemcbxNvk7vgbLP0wc-p-7Nq3oCTQC3FQ7ZrTRPpaDMP2P3o9K48T8c3ZxflyTit8iEWqZIkTS6VkFMitKIghQVkQhacgxlyCbUwOBXcFkUBpsqVRVXZ_jWqTY3T7IB9Xd9dBP-4pNjpmV-Gto_UiBIzrlQme-rbhjKxMo0Npq1c1Ivg5iasNBcyGyoUPTdYc1XwMQayWwRBvxaqXwvV20J7If8gVK57q6cLxjX_1tRae3INrf4Tok8vb8r3brp2Xezoeeua8Ff3b8ihfrg-0z_U5Pvo8vaXnmQvjp-bNQ |
| CitedBy_id | crossref_primary_10_1002_ange_201807873 crossref_primary_10_1021_acs_orglett_7b02601 crossref_primary_10_1002_asia_202100693 crossref_primary_10_1002_cjoc_201500889 crossref_primary_10_1002_adsc_201400057 crossref_primary_10_1039_D4QO00433G crossref_primary_10_1080_16583655_2018_1465265 crossref_primary_10_1039_C4CC04487H crossref_primary_10_1002_ajoc_202000170 crossref_primary_10_1021_jacs_6b10468 crossref_primary_10_1039_c3nj00044c crossref_primary_10_1002_adsc_201400504 crossref_primary_10_1002_ejoc_201800291 crossref_primary_10_1021_acs_orglett_8b02128 crossref_primary_10_1002_ajoc_201600348 crossref_primary_10_1016_j_jfluchem_2015_09_015 crossref_primary_10_1002_ange_201709663 crossref_primary_10_1002_ejoc_201301512 crossref_primary_10_1021_acs_joc_4c01900 crossref_primary_10_1021_acs_organomet_5b00350 crossref_primary_10_1002_ange_201304276 crossref_primary_10_1002_anie_201208971 crossref_primary_10_1039_C6DT00277C crossref_primary_10_1007_s11244_018_0973_7 crossref_primary_10_1021_acs_joc_9b02254 crossref_primary_10_1039_C4OB02145B crossref_primary_10_1002_anie_201500899 crossref_primary_10_1002_ejoc_201600074 crossref_primary_10_1039_C6RA10302B crossref_primary_10_1016_j_tetlet_2022_153717 crossref_primary_10_1021_ja507564p crossref_primary_10_1039_D3QO00493G crossref_primary_10_1002_adsc_201601298 crossref_primary_10_1021_acs_orglett_3c00206 crossref_primary_10_1039_C4QO00240G crossref_primary_10_1016_j_jfluchem_2013_06_007 crossref_primary_10_3762_bjoc_11_286 crossref_primary_10_1016_j_ccr_2013_07_004 crossref_primary_10_1039_C9QO00527G crossref_primary_10_1021_ol503189j crossref_primary_10_1002_chem_201402098 crossref_primary_10_1016_j_tetlet_2018_05_004 crossref_primary_10_1002_ange_201302673 crossref_primary_10_1021_acscatal_0c03776 crossref_primary_10_1002_asia_201500359 crossref_primary_10_1039_D2OB00894G crossref_primary_10_1002_anie_201501880 crossref_primary_10_1016_j_tet_2016_04_048 crossref_primary_10_1021_ol501967c crossref_primary_10_1002_ange_201309260 crossref_primary_10_1002_chem_201502914 crossref_primary_10_1021_acs_orglett_5b02184 crossref_primary_10_1002_anie_201306082 crossref_primary_10_1002_cjoc_202200230 crossref_primary_10_1002_tcr_202100231 crossref_primary_10_1039_C8QO01118D crossref_primary_10_1021_acs_joc_5b01295 crossref_primary_10_1021_acs_joc_3c00621 crossref_primary_10_1039_C9OB01865D crossref_primary_10_1039_C4RA03199G crossref_primary_10_1002_ange_201301891 crossref_primary_10_1016_j_jfluchem_2020_109516 crossref_primary_10_1016_j_tet_2014_09_091 crossref_primary_10_1002_anie_201709663 crossref_primary_10_1002_ejoc_201901929 crossref_primary_10_1002_ange_201208971 crossref_primary_10_1002_adsc_201800275 crossref_primary_10_1002_chem_201504306 crossref_primary_10_1002_ange_201904041 crossref_primary_10_1002_cjoc_201500730 crossref_primary_10_1007_s11030_024_11017_1 crossref_primary_10_1038_ncomms4387 crossref_primary_10_1039_C5RA07316B crossref_primary_10_1002_ange_201704175 crossref_primary_10_1016_j_tetlet_2017_08_038 crossref_primary_10_1016_j_ccr_2014_11_004 crossref_primary_10_1021_ol5001395 crossref_primary_10_1039_C6QO00156D crossref_primary_10_1016_j_tetlet_2022_154100 crossref_primary_10_1055_a_1709_3098 crossref_primary_10_1021_acs_orglett_5b02522 crossref_primary_10_1021_ja504458j crossref_primary_10_1016_j_jfluchem_2018_10_003 crossref_primary_10_1016_j_tet_2016_04_081 crossref_primary_10_1021_cr500410y crossref_primary_10_1021_jo502928e crossref_primary_10_1039_C6CC09905J crossref_primary_10_1016_j_jfluchem_2021_109930 crossref_primary_10_1002_chem_202000856 crossref_primary_10_1021_jo500713f crossref_primary_10_1039_D2QO00285J crossref_primary_10_1002_cjoc_201400427 crossref_primary_10_1002_chem_201503915 crossref_primary_10_1021_ol5030037 crossref_primary_10_1021_acs_joc_6b01739 crossref_primary_10_1002_anie_201309260 crossref_primary_10_1021_acs_orglett_9b03012 crossref_primary_10_1021_jacs_5b10971 crossref_primary_10_1002_adsc_201701051 crossref_primary_10_1002_anie_201301891 crossref_primary_10_1021_om500472b crossref_primary_10_1039_C6QO00166A crossref_primary_10_1002_chem_201602920 crossref_primary_10_1021_acs_organomet_8b00579 crossref_primary_10_1021_acscatal_4c07840 crossref_primary_10_1039_D4QO00600C crossref_primary_10_1021_acs_orglett_3c02804 crossref_primary_10_1021_acs_orglett_5b01170 crossref_primary_10_1021_acs_orglett_0c01206 crossref_primary_10_1002_chem_201503524 crossref_primary_10_1016_j_ccr_2022_214455 crossref_primary_10_13005_ojc_340603 crossref_primary_10_1039_C5SC03636D crossref_primary_10_1016_j_molstruc_2024_138350 crossref_primary_10_1021_acs_joc_1c00361 crossref_primary_10_1002_ange_201500899 crossref_primary_10_1002_anie_201704175 crossref_primary_10_1002_ejoc_201600578 crossref_primary_10_1021_acs_orglett_5b01616 crossref_primary_10_1039_C4QO00173G crossref_primary_10_1021_ol501742a crossref_primary_10_1021_acs_oprd_1c00381 crossref_primary_10_1002_anie_201304276 crossref_primary_10_1002_ejoc_201801662 crossref_primary_10_1021_acs_orglett_0c02300 crossref_primary_10_1039_c3cc43120g crossref_primary_10_1002_adsc_201801681 crossref_primary_10_1021_acs_joc_6b03012 crossref_primary_10_1002_ejoc_202300253 crossref_primary_10_1021_acs_orglett_6b00168 crossref_primary_10_1002_adsc_201400340 crossref_primary_10_1002_anie_201904041 crossref_primary_10_1039_C8QO00499D crossref_primary_10_1002_chin_201315231 crossref_primary_10_1016_j_jfluchem_2015_03_009 crossref_primary_10_1021_acs_orglett_5b01510 crossref_primary_10_1039_C6CC00666C crossref_primary_10_1039_c3sc53076k crossref_primary_10_1039_C5CC01923K crossref_primary_10_1002_chem_201302328 crossref_primary_10_1016_j_jfluchem_2014_06_015 crossref_primary_10_1002_anie_202002409 crossref_primary_10_1021_ol5030184 crossref_primary_10_1016_j_jfluchem_2014_05_009 crossref_primary_10_1002_ejoc_201800325 crossref_primary_10_1002_chem_201602730 crossref_primary_10_1002_anie_201807873 crossref_primary_10_1002_ange_201501880 crossref_primary_10_1039_C8QO01249K crossref_primary_10_1002_ange_201306082 crossref_primary_10_1021_ol5018195 crossref_primary_10_1021_acs_joc_4c00557 crossref_primary_10_1002_ejoc_202401023 crossref_primary_10_1016_j_jfluchem_2014_06_026 crossref_primary_10_1021_cr400473a crossref_primary_10_1002_ejoc_201402526 crossref_primary_10_1039_C6DT03016E crossref_primary_10_1021_ol4026827 crossref_primary_10_6023_cjoc202107042 crossref_primary_10_1002_cjoc_201600888 crossref_primary_10_1002_ange_201505335 crossref_primary_10_1002_ange_201506329 crossref_primary_10_1002_chem_201805526 crossref_primary_10_1002_ajoc_201300236 crossref_primary_10_1002_ejoc_201300473 crossref_primary_10_1021_acs_joc_8b00927 crossref_primary_10_3762_bjoc_9_287 crossref_primary_10_1002_anie_201302673 crossref_primary_10_1002_cjoc_201300393 crossref_primary_10_1002_ejoc_201403221 crossref_primary_10_1039_D0QO00955E crossref_primary_10_1021_cr500223h crossref_primary_10_1039_D2OB00483F crossref_primary_10_1021_jo501289v crossref_primary_10_1021_jacs_5b02046 crossref_primary_10_1021_jo4023233 crossref_primary_10_1002_anie_201505335 crossref_primary_10_1021_acs_orglett_5b01024 crossref_primary_10_1016_j_jfluchem_2019_109359 crossref_primary_10_1002_ajoc_201500096 crossref_primary_10_1021_acs_orglett_5b01027 crossref_primary_10_1021_ol400122k crossref_primary_10_1002_aoc_5303 crossref_primary_10_1002_ejoc_201403115 crossref_primary_10_1021_ol502921a crossref_primary_10_1002_ange_202002409 crossref_primary_10_1002_slct_202103407 crossref_primary_10_1021_acs_orglett_1c02136 crossref_primary_10_1021_jacs_1c07408 crossref_primary_10_1021_cr5002386 crossref_primary_10_1002_tcr_202300124 crossref_primary_10_1016_j_jfluchem_2013_03_009 crossref_primary_10_1002_ejoc_201400087 crossref_primary_10_1002_ange_201500341 crossref_primary_10_1002_ejoc_201501189 crossref_primary_10_1002_chem_201403447 crossref_primary_10_1039_C9QO01436E crossref_primary_10_1021_acs_orglett_2c00637 crossref_primary_10_1021_cr500257c crossref_primary_10_1002_ejoc_202400304 crossref_primary_10_1039_C5RA02279G crossref_primary_10_1002_tcr_202300154 crossref_primary_10_1021_acs_joc_4c00227 crossref_primary_10_1038_s41467_024_52035_9 crossref_primary_10_1002_asia_202400331 crossref_primary_10_1016_j_tetlet_2014_01_061 crossref_primary_10_1039_D4SC02075H crossref_primary_10_1039_C4OB01088D crossref_primary_10_1039_C5RA11337G crossref_primary_10_1021_ol502331a crossref_primary_10_1039_C8SC03754J crossref_primary_10_1039_C6RA15547B crossref_primary_10_1002_anie_201500341 crossref_primary_10_1039_C6CP07093K crossref_primary_10_1002_anie_201506329 crossref_primary_10_1039_C6RA09011G crossref_primary_10_3762_bjoc_14_11 crossref_primary_10_1002_ejoc_202400899 crossref_primary_10_1002_adsc_201500731 crossref_primary_10_1016_j_jfluchem_2015_06_001 crossref_primary_10_1021_jo501221h crossref_primary_10_1039_C6QO00194G crossref_primary_10_1016_j_jfluchem_2014_09_013 crossref_primary_10_1021_acs_joc_5b01468 |
| Cites_doi | 10.1016/S0022-1139(00)80126-8 10.1126/science.1190524 10.1021/ja200314m 10.2174/157017910792246081 10.2174/157017910792246117 10.1002/anie.201106668 10.1021/ja909522s 10.1021/jo202566h 10.1021/jo1023377 10.1021/ja2041942 10.1021/ol1023135 10.1002/9780470281895 10.1038/nature10647 10.1002/adsc.201000825 10.1021/ar7002573 10.1039/C39930001389 10.1021/ja201726q 10.1039/c1cc13460d 10.1073/pnas.1109059108 10.1021/om200204y 10.1021/ja064935c 10.1016/j.jfluchem.2009.10.011 10.1002/cjoc.19930110411 10.1039/c39890000705 10.1002/9780470988589 10.1021/ar700149s 10.1055/s-0030-1260930 10.1016/S0022-1139(00)80112-8 10.1002/3527606548 10.1021/cr00039a007 10.1021/om800794m 10.1021/ol2005903 10.1016/j.tetlet.2010.09.027 10.1016/j.jfluchem.2010.06.020 10.1016/S0040-4039(00)74267-5 10.1021/ja0602389 10.1039/b823249k 10.1016/j.tet.2011.01.002 10.1246/cl.1981.1719 10.1021/ja802946s 10.1002/anie.201101577 10.1055/s-1980-29276 10.1021/ja2081026 10.1016/S0040-4020(01)80011-9 10.1002/352760393X 10.1021/ja301553c 10.1002/anie.201006823 10.1021/ja100955x 10.1016/S0040-4039(00)71226-3 10.1038/nature10108 10.1126/science.1131943 10.1002/chem.201100283 10.1016/S0040-4039(01)88624-X 10.1002/chem.201102652 10.1021/ja00303a042 10.1002/anie.201100633 10.1016/S0040-4020(01)83100-8 10.3762/bjoc.6.65 10.1002/anie.201106673 10.1021/cr1004293 10.1002/chem.201002749 10.1039/c1cc10359h 10.1016/0022-1139(93)03014-D 10.1016/j.jfluchem.2011.07.025 10.1039/B610213C 10.1002/anie.201004051 10.1021/ja00264a043 10.1002/ejoc.201101535 10.1002/anie.201201012 10.1021/ol201205t |
| ContentType | Journal Article |
| Copyright | Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim 2014 INIST-CNRS Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| Copyright_xml | – notice: Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: 2014 INIST-CNRS – notice: Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| DBID | BSCLL AAYXX CITATION IQODW |
| DOI | 10.1002/ejoc.201200648 |
| DatabaseName | Istex CrossRef Pascal-Francis |
| DatabaseTitle | CrossRef |
| DatabaseTitleList | CrossRef |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1099-0690 |
| EndPage | 6687 |
| ExternalDocumentID | 2819421061 26735916 10_1002_ejoc_201200648 EJOC201200648 ark_67375_WNG_R9PBFJSZ_P |
| Genre | reviewArticle |
| GroupedDBID | -~X .3N .GA .Y3 05W 0R~ 10A 1L6 1OC 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5VS 66C 702 77Q 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AABCJ AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABDBF ABEML ABIJN ABJNI ABLJU ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACIWK ACNCT ACPOU ACSCC ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFZJQ AHBTC AI. AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ATUGU AUFTA AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BY8 CS3 D-E D-F DCZOG DPXWK DR2 DRFUL DRSTM EBS EJD F00 F01 F04 F5P FEDTE G-S G.N GNP GODZA H.T H.X HBH HF~ HGLYW HHY HHZ HVGLF HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MVM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 SUPJJ TN5 UB1 UPT V2E VH1 W8V W99 WBFHL WBKPD WH7 WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XJT XOL XPP XV2 ZCG ~IA ~WT AAHQN AAMNL AANHP AAYCA ACRPL ACUHS ACYXJ ADNMO AFWVQ ALVPJ AAYXX AEYWJ AGHNM AGQPQ AGYGG CITATION AAMMB AEFGJ AGXDD AIDQK AIDYY IQODW 1OB |
| ID | FETCH-LOGICAL-c4518-97e7a47967bee1f68e91803678220a5270d6a1b62f8880ac49f19cf002edad1b3 |
| IEDL.DBID | DR2 |
| ISSN | 1434-193X |
| IngestDate | Wed Aug 13 06:24:15 EDT 2025 Mon Jul 21 09:12:18 EDT 2025 Tue Jul 01 03:23:49 EDT 2025 Thu Apr 24 22:58:27 EDT 2025 Wed Jan 22 16:26:38 EST 2025 Wed Oct 30 09:51:47 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 34 |
| Keywords | Arene Catalytic reaction Copper ion Trifluoromethylation Mild operating conditions Fluorine Arenes Aromatic compound Transition metal Copper |
| Language | English |
| License | CC BY 4.0 |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c4518-97e7a47967bee1f68e91803678220a5270d6a1b62f8880ac49f19cf002edad1b3 |
| Notes | ArticleID:EJOC201200648 ark:/67375/WNG-R9PBFJSZ-P istex:557C494A5469BAE84BB56CCD57DE13E244760BD1 ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 |
| PQID | 1171329937 |
| PQPubID | 986364 |
| PageCount | 9 |
| ParticipantIDs | proquest_journals_1171329937 pascalfrancis_primary_26735916 crossref_primary_10_1002_ejoc_201200648 crossref_citationtrail_10_1002_ejoc_201200648 wiley_primary_10_1002_ejoc_201200648_EJOC201200648 istex_primary_ark_67375_WNG_R9PBFJSZ_P |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | December 2012 |
| PublicationDateYYYYMMDD | 2012-12-01 |
| PublicationDate_xml | – month: 12 year: 2012 text: December 2012 |
| PublicationDecade | 2010 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim |
| PublicationTitle | European journal of organic chemistry |
| PublicationTitleAlternate | Eur. J. Org. Chem |
| PublicationYear | 2012 |
| Publisher | WILEY-VCH Verlag WILEY‐VCH Verlag Wiley-VCH Wiley Subscription Services, Inc |
| Publisher_xml | – name: WILEY-VCH Verlag – name: WILEY‐VCH Verlag – name: Wiley-VCH – name: Wiley Subscription Services, Inc |
| References | J. P. Bégué , D. Bonnet-Delpon , Bioorganic and Medicinal Chemistry of Fluorine, Wiley-Interscience, New Jersey, 2008 . T. D. Senecal , A. T. Parsons , S. L. Buchwald , J. Org. Chem. 2011 , 76 , 1174 . K. Uneyama , T. Katagiri , H. Amii , Acc. Chem. Res. 2008 , 41 , 817 . R. J. Lundgren , M. Stradiotto , Angew. Chem. Int. Ed. 2010 , 49 , 9322 . L. Chu , F.-L. Qing , J. Am. Chem. Soc. 2011 , 133 , 1298 . O. A. Tomashenko , V. V. Grushin , Chem. Rev. 2011 , 111 , 4475 . S. Roy , B. T. Gregg , G. W. Gribble , V.-D. Le , S. Roy , Tetrahedron 2011 , 67 , 2161 . Y. Ye , M. S. Sanford , J. Am. Chem. Soc. 2012 , 134 , 9034 . J. H. Clark , D. Wails , T. W. Bastock , Aromatic Fluorination, CRC Press, Boca Raton, 1996 . Q.-Y. Chen , S.-W. Wu , J. Chem. Soc., Chem. Commun. 1989 , 705 . D. J. Burton , in: Chemistry of Organocopper Compounds (Eds.: Z. Rappoport , I. Marek) , Wiley, Chichester, UK, 2009 . E. J. Cho , T. D. Senecal , T. Kinzel , Y. Zhang , D. A. Watson , S. L. Buchwald , Science 2010 , 328 , 1679 . V. V. Grushin , W. J. Marshall , J. Am. Chem. Soc. 2006 , 128 , 4632 . D. J. Burton , D. M. Wiemers , J. Am. Chem. Soc. 1985 , 107 , 5014 . H.-D. Li , J.-X. Duan , D.-B. Su , Q.-Y. Chen , Chin. J. Chem. 1993 , 11 , 366 . J.-X. Duan , D.-B. Su , Q.-Y. Chen , J. Fluorine Chem. 1993 , 61 , 279 . V. C. R. McLoughlin , J. Thrower , Tetrahedron 1969 , 25 , 5921 . Y. Macé , E. Magnier , Eur. J. Org. Chem. 2012 , 13 , 2479 . X. Wang , L. Truesdale , J.-Q. Yu , J. Am. Chem. Soc. 2010 , 132 , 3648 . Y. Ji , T. Brueckl , R. Baxter , Y. Fujiwara , I. B. Seiple , S. Su , D. G. Blackmond , P. S. Baran , Proc. Natl. Acad. Sci. USA 2011 , 108 , 14411 . N. V. Kondratenko , E. P. Vechirko , L. M. Yagupolskii , Synthesis 1980 , 932 . A. H. M. Elwahy, M. R. Shaaban , Curr. Org. Synth. 2010 , 7 , 433 . R. Shimizu , H. Egami , T. Nagi , J. Chae , Y. Hamashima , M. Sodeoka , Tetrahedron Lett. 2010 , 51 , 5947 . H. Kawai , T. Furukawa , Y. Nomura , E. Tokunaga , N. Shibata , Org. Lett. 2011 , 13 , 3596 . A. S. Abreu , P. M. T. Ferreira , M. J. R. P. Queiroz, Suzuki Coupling Reactions, in: Catalysts for Fine Chemical Synthesis: Metal Catalysed Carbon-Carbon Bond-Forming Reactions, vol. 3 (Eds.: S. M. Roberts , J. Xiao , J. Whittall , T. E. Pickett) , Wiley, Chichester, UK, 2005 . J. Tsuji , Palladium Reagents and Catalysts: New Perspectives for the 21st Century, Wiley, Chichester, UK, 2003 . N. D. Ball , J. W. Kampf , M. S. Sanford , J. Am. Chem. Soc. 2010 , 132 , 2878 . T. Basset , C. Schneider , D. Cahard , Angew. Chem. Int. Ed. 2012 , 51 , 5048 . M. M. Kremlev , W. Tyrra , A. I. Mushta , D. Naumann , Y. L. Yagupolskii , J. Fluorine Chem. 2010 , 131 , 212 . J.-X. Duan , D.-B. Su , J.-P. Wu , Q.-Y. Chen , J. Fluorine Chem. 1994 , 66 , 167 . P. Kirsch , Modern Fluoroorganic Chemistry, Wiley-VCH, Weinheim, Germany, 2004 . H. Morimoto , T. Tsubogo , N. D. Litvinas , J. F. Hartwig , Angew. Chem. Int. Ed. 2011 , 50 , 3793 . K. Müller , C. Faeh , F. Diederich , Science 2007 , 317 , 1881 . G. G. Dubinina , H. Furutachi , D. A. Vicic , J. Am. Chem. Soc. 2008 , 130 , 8600 . C.-P. Zhang , Z.-L. Wang , Q.-Y. Chen , C.-T. Zhang , Y.-C. Gu , J.-C. Xiao , Angew. Chem. Int. Ed. 2011 , 50 , 1896 . X. Jiang , L. Chu , F.-L. Qing , J. Org. Chem. 2012 , 77 , 1251 . T. Knauber , F. G. R. Arikan , L. J. Gooßen , Chem. Eur. J. 2011 , 17 , 2689 . D. M. Wiemers , D. J. Burton , J. Am. Chem. Soc. 1986 , 108 , 832 . I. Popov , S. Lindeman , O. Daugulis , J. Am. Chem. Soc. 2011 , 133 , 9286 . H. Urata , T. Fuchikami , Tetrahedron Lett. 1991 , 32 , 91 . H. Kondo , M. Oishi , K. Fujikawa , H. Amii , Adv. Synth. Catal. 2011 , 353 , 1247 . G. G. Dubinina , J. Ogikubo , D. A. Vicic , Organometallics 2008 , 27 , 6233 . S. Purser , P. R. Moore , S. Swallow , V. Gouverneur , Chem. Soc. Rev. 2008 , 37 , 320 . N. D. Litvinas , P. S. Fier , J. F. Hartwig , Angew. Chem. Int. Ed. 2012 , 51 , 536 . M. S. Miehn , E. Vinogradova , A. Togni , J. Fluorine Chem. 2010 , 131 , 951 . M. Oishi , H. Kondo , H. Amii , Chem. Commun. 2009 , 1909 . N. Miyaura , A. Suzuki , Chem. Rev. 1995 , 95 , 2457 -2483 . Q.-Y. Chen , J.-X. Duan , J. Chem. Soc., Chem. Commun. 1993 , 1389 . N. Boechat , M. M. Bastos , Curr. Org. Synth. 2010 , 7 , 403 . O. A. Tomashenko , E. C. Escudero-Adan , M. Martinez Belmonte , V. V. Grushin , Angew. Chem. Int. Ed. 2011 , 50 , 7655 . J. Xu , D.-F. Luo , B. Xiao , Z.-J. Liu , T.-J. Gong , Y. Fu , L. Liu , Chem. Commun. 2011 , 47 , 4300 . Y. Li , T. Chen , H. Wang , R. Zhang , K. Jin , X. Wang , C. Duan , Synlett 2011 , 1713 . L. Chu , F.-L. Qing , Org. Lett. 2010 , 12 , 5060 . T. Liu , X. Shao , Y. Wu , Q. Shen , Angew. Chem. Int. Ed. 2012 , 51 , 540 . Z. Weng , R. Lee , W. Jia , Y. Yuan , W. Wang , X. Feng , K.-W. Huang , Organometallics 2011 , 30 , 3229 . Y. Kobayashi , I. Kumadaki , Tetrahedron Lett. 1969 , 10 , 4095 . N. Shibata , A. Matsnev , D. Cahard , Beilstein J. Org. Chem. 2010 , 6 , 65 . B. A. Khan , A. E. Buba , L. J. Gooßen , Chem. Eur. J. 2012 , 18 , 1577 . C.-P. Zhang , J. Cai , C.-B. Zhou , X.-P. Wang , X. Zheng , Y.-C. Gu , J.-C. Xiao , Chem. Commun. 2011 , 47 , 9516 . G. K. S. Prakash, J. Hu , Acc. Chem. Res. 2007 , 40 , 921 . T. Liu , Q. Shen , Org. Lett. 2011 , 13 , 2342 . X. Mu , S. Chen , X. Zheng , G. Liu , Chem. Eur. J. 2011 , 17 , 6039 . A. Zanardi , M. A. Novikov , E. Martin , J. Benet-Buchholz , V. V. Grushin , J. Am. Chem. Soc. 2011 , 133 , 20901 . N. D. Ball , J. B. Gary , Y. Ye , M. S. Sanford , J. Am. Chem. Soc. 2011 , 133 , 7577 . V. V. Grushin , W. J. Marshall , J. Am. Chem. Soc. 2006 , 128 , 12644 . K. Uneyama , Organofluorine Chemistry, Blackwell, Oxford, UK, 2006 . T. Furuya , A. S. Kamlet , T. Ritter , Nature 2011 , 473 , 470 . M. A. McClinton , D. A. McClinton , Tetrahedron 1992 , 48 , 6555 . D. A. Nagib , D. W. C. MacMillan , Nature 2011 , 480 , 224 . J. G. MacNeil Jr , D. J. Burton , J. Fluorine Chem. 1991 , 55 , 225 . K. Matsui , E. Tobita , M. Ando , K. Kondo , Chem. Lett. 1981 , 10 , 1719 . D. B. Su , J. X. Duan , Q. Y. Chen , Tetrahedron Lett. 1991 , 32 , 7689 . M. M. Kremlev , A. I. Mushta , W. Tyrra , Y. L. Yagupolskii , D. Naumann , A. Möller , J. Fluorine Chem. 2012 , 133 , 67 . D. G. Hall , Boronic Acids, Wiley-VCH, Weinheim, Germany, 2005 . 2010; 12 1993; 61 1991; 55 2008; 37 1994; 66 2012; 18 2011; 13 2011; 17 2012; 13 2011; 111 2011; 353 2011; 473 2012; 51 1986; 108 2012; 133 2012; 134 2008; 27 2011; 67 1992; 48 1980 2011; 480 2006; 128 2010; 7 2010; 6 1989 1995; 95 2010; 328 2011 1991; 32 1969; 10 2009 2008 2011; 30 1996 2006 2011; 76 2005 1993 2004 1985; 107 2003 2012; 77 2011; 133 2010; 49 2007; 317 2011; 108 1993; 11 2011; 50 2010; 132 1969; 25 2010; 131 2008; 41 2007; 40 2011; 47 1981; 10 2008; 130 1968 2010; 51 e_1_2_7_5_2 e_1_2_7_3_2 e_1_2_7_9_2 e_1_2_7_7_2 e_1_2_7_19_2 e_1_2_7_17_2 e_1_2_7_15_2 e_1_2_7_60_2 e_1_2_7_81_2 e_1_2_7_1_2 e_1_2_7_13_2 e_1_2_7_41_2 e_1_2_7_62_2 Clark J. H. (e_1_2_7_2_2) 1996 e_1_2_7_11_2 e_1_2_7_43_2 e_1_2_7_64_2 e_1_2_7_45_2 e_1_2_7_66_2 e_1_2_7_47_2 e_1_2_7_26_2 e_1_2_7_49_2 e_1_2_7_28_2 e_1_2_7_71_2 Burton D. J. (e_1_2_7_44_2) 2009 e_1_2_7_50_2 e_1_2_7_25_2 e_1_2_7_75_2 e_1_2_7_23_2 e_1_2_7_54_2 e_1_2_7_73_2 e_1_2_7_21_2 e_1_2_7_33_2 e_1_2_7_56_2 e_1_2_7_79_2 e_1_2_7_35_2 e_1_2_7_58_2 e_1_2_7_77_2 e_1_2_7_37_2 e_1_2_7_39_2 e_1_2_7_4_2 Tsuji J. (e_1_2_7_68_2) 2003 e_1_2_7_8_2 e_1_2_7_6_2 e_1_2_7_18_2 e_1_2_7_82_2 e_1_2_7_16_2 e_1_2_7_61_2 e_1_2_7_80_2 e_1_2_7_14_2 e_1_2_7_40_2 e_1_2_7_63_2 e_1_2_7_12_2 e_1_2_7_42_2 e_1_2_7_65_2 e_1_2_7_10_2 e_1_2_7_46_2 e_1_2_7_69_2 e_1_2_7_48_2 e_1_2_7_27_2 e_1_2_7_29_2 Abreu A. S. (e_1_2_7_67_2) 2005 e_1_2_7_72_2 e_1_2_7_70_2 e_1_2_7_24_2 e_1_2_7_30_2 Li H.‐D. (e_1_2_7_31_2) 1993; 11 e_1_2_7_51_2 e_1_2_7_76_2 e_1_2_7_22_2 e_1_2_7_32_2 e_1_2_7_53_2 e_1_2_7_74_2 e_1_2_7_20_2 e_1_2_7_34_2 e_1_2_7_55_2 e_1_2_7_36_2 e_1_2_7_57_2 e_1_2_7_78_2 e_1_2_7_38_2 e_1_2_7_59_2 Hu J. (e_1_2_7_52_2) 2007; 40 |
| References_xml | – reference: T. Basset , C. Schneider , D. Cahard , Angew. Chem. Int. Ed. 2012 , 51 , 5048 . – reference: T. Liu , Q. Shen , Org. Lett. 2011 , 13 , 2342 . – reference: D. J. Burton , D. M. Wiemers , J. Am. Chem. Soc. 1985 , 107 , 5014 . – reference: N. Boechat , M. M. Bastos , Curr. Org. Synth. 2010 , 7 , 403 . – reference: A. H. M. Elwahy, M. R. Shaaban , Curr. Org. Synth. 2010 , 7 , 433 . – reference: N. V. Kondratenko , E. P. Vechirko , L. M. Yagupolskii , Synthesis 1980 , 932 . – reference: N. Shibata , A. Matsnev , D. Cahard , Beilstein J. Org. Chem. 2010 , 6 , 65 . – reference: I. Popov , S. Lindeman , O. Daugulis , J. Am. Chem. Soc. 2011 , 133 , 9286 . – reference: L. Chu , F.-L. Qing , J. Am. Chem. Soc. 2011 , 133 , 1298 . – reference: R. J. Lundgren , M. Stradiotto , Angew. Chem. Int. Ed. 2010 , 49 , 9322 . – reference: X. Mu , S. Chen , X. Zheng , G. Liu , Chem. Eur. J. 2011 , 17 , 6039 . – reference: H. Urata , T. Fuchikami , Tetrahedron Lett. 1991 , 32 , 91 . – reference: K. Uneyama , Organofluorine Chemistry, Blackwell, Oxford, UK, 2006 . – reference: B. A. Khan , A. E. Buba , L. J. Gooßen , Chem. Eur. J. 2012 , 18 , 1577 . – reference: J.-X. Duan , D.-B. Su , Q.-Y. Chen , J. Fluorine Chem. 1993 , 61 , 279 . – reference: K. Uneyama , T. Katagiri , H. Amii , Acc. Chem. Res. 2008 , 41 , 817 . – reference: T. Knauber , F. G. R. Arikan , L. J. Gooßen , Chem. Eur. J. 2011 , 17 , 2689 . – reference: N. D. Ball , J. W. Kampf , M. S. Sanford , J. Am. Chem. Soc. 2010 , 132 , 2878 . – reference: D. J. Burton , in: Chemistry of Organocopper Compounds (Eds.: Z. Rappoport , I. Marek) , Wiley, Chichester, UK, 2009 . – reference: J. G. MacNeil Jr , D. J. Burton , J. Fluorine Chem. 1991 , 55 , 225 . – reference: J. Tsuji , Palladium Reagents and Catalysts: New Perspectives for the 21st Century, Wiley, Chichester, UK, 2003 . – reference: H. Morimoto , T. Tsubogo , N. D. Litvinas , J. F. Hartwig , Angew. Chem. Int. Ed. 2011 , 50 , 3793 . – reference: Q.-Y. Chen , J.-X. Duan , J. Chem. Soc., Chem. Commun. 1993 , 1389 . – reference: Y. Kobayashi , I. Kumadaki , Tetrahedron Lett. 1969 , 10 , 4095 . – reference: O. A. Tomashenko , E. C. Escudero-Adan , M. Martinez Belmonte , V. V. Grushin , Angew. Chem. Int. Ed. 2011 , 50 , 7655 . – reference: N. Miyaura , A. Suzuki , Chem. Rev. 1995 , 95 , 2457 -2483 . – reference: J.-X. Duan , D.-B. Su , J.-P. Wu , Q.-Y. Chen , J. Fluorine Chem. 1994 , 66 , 167 . – reference: G. G. Dubinina , J. Ogikubo , D. A. Vicic , Organometallics 2008 , 27 , 6233 . – reference: X. Jiang , L. Chu , F.-L. Qing , J. Org. Chem. 2012 , 77 , 1251 . – reference: H. Kawai , T. Furukawa , Y. Nomura , E. Tokunaga , N. Shibata , Org. Lett. 2011 , 13 , 3596 . – reference: E. J. Cho , T. D. Senecal , T. Kinzel , Y. Zhang , D. A. Watson , S. L. Buchwald , Science 2010 , 328 , 1679 . – reference: D. A. Nagib , D. W. C. MacMillan , Nature 2011 , 480 , 224 . – reference: H.-D. Li , J.-X. Duan , D.-B. Su , Q.-Y. Chen , Chin. J. Chem. 1993 , 11 , 366 . – reference: Z. Weng , R. Lee , W. Jia , Y. Yuan , W. Wang , X. Feng , K.-W. Huang , Organometallics 2011 , 30 , 3229 . – reference: Y. Ji , T. Brueckl , R. Baxter , Y. Fujiwara , I. B. Seiple , S. Su , D. G. Blackmond , P. S. Baran , Proc. Natl. Acad. Sci. USA 2011 , 108 , 14411 . – reference: K. Matsui , E. Tobita , M. Ando , K. Kondo , Chem. Lett. 1981 , 10 , 1719 . – reference: M. M. Kremlev , A. I. Mushta , W. Tyrra , Y. L. Yagupolskii , D. Naumann , A. Möller , J. Fluorine Chem. 2012 , 133 , 67 . – reference: T. D. Senecal , A. T. Parsons , S. L. Buchwald , J. Org. Chem. 2011 , 76 , 1174 . – reference: Y. Li , T. Chen , H. Wang , R. Zhang , K. Jin , X. Wang , C. Duan , Synlett 2011 , 1713 . – reference: Q.-Y. Chen , S.-W. Wu , J. Chem. Soc., Chem. Commun. 1989 , 705 . – reference: H. Kondo , M. Oishi , K. Fujikawa , H. Amii , Adv. Synth. Catal. 2011 , 353 , 1247 . – reference: D. M. Wiemers , D. J. Burton , J. Am. Chem. Soc. 1986 , 108 , 832 . – reference: G. G. Dubinina , H. Furutachi , D. A. Vicic , J. Am. Chem. Soc. 2008 , 130 , 8600 . – reference: Y. Ye , M. S. Sanford , J. Am. Chem. Soc. 2012 , 134 , 9034 . – reference: P. Kirsch , Modern Fluoroorganic Chemistry, Wiley-VCH, Weinheim, Germany, 2004 . – reference: O. A. Tomashenko , V. V. Grushin , Chem. Rev. 2011 , 111 , 4475 . – reference: D. B. Su , J. X. Duan , Q. Y. Chen , Tetrahedron Lett. 1991 , 32 , 7689 . – reference: V. V. Grushin , W. J. Marshall , J. Am. Chem. Soc. 2006 , 128 , 4632 . – reference: A. Zanardi , M. A. Novikov , E. Martin , J. Benet-Buchholz , V. V. Grushin , J. Am. Chem. Soc. 2011 , 133 , 20901 . – reference: J. H. Clark , D. Wails , T. W. Bastock , Aromatic Fluorination, CRC Press, Boca Raton, 1996 . – reference: S. Roy , B. T. Gregg , G. W. Gribble , V.-D. Le , S. Roy , Tetrahedron 2011 , 67 , 2161 . – reference: A. S. Abreu , P. M. T. Ferreira , M. J. R. P. Queiroz, Suzuki Coupling Reactions, in: Catalysts for Fine Chemical Synthesis: Metal Catalysed Carbon-Carbon Bond-Forming Reactions, vol. 3 (Eds.: S. M. Roberts , J. Xiao , J. Whittall , T. E. Pickett) , Wiley, Chichester, UK, 2005 . – reference: L. Chu , F.-L. Qing , Org. Lett. 2010 , 12 , 5060 . – reference: N. D. Litvinas , P. S. Fier , J. F. Hartwig , Angew. Chem. Int. Ed. 2012 , 51 , 536 . – reference: Y. Macé , E. Magnier , Eur. J. Org. Chem. 2012 , 13 , 2479 . – reference: M. S. Miehn , E. Vinogradova , A. Togni , J. Fluorine Chem. 2010 , 131 , 951 . – reference: S. Purser , P. R. Moore , S. Swallow , V. Gouverneur , Chem. Soc. Rev. 2008 , 37 , 320 . – reference: C.-P. Zhang , Z.-L. Wang , Q.-Y. Chen , C.-T. Zhang , Y.-C. Gu , J.-C. Xiao , Angew. Chem. Int. Ed. 2011 , 50 , 1896 . – reference: X. Wang , L. Truesdale , J.-Q. Yu , J. Am. Chem. Soc. 2010 , 132 , 3648 . – reference: R. Shimizu , H. Egami , T. Nagi , J. Chae , Y. Hamashima , M. Sodeoka , Tetrahedron Lett. 2010 , 51 , 5947 . – reference: M. M. Kremlev , W. Tyrra , A. I. Mushta , D. Naumann , Y. L. Yagupolskii , J. Fluorine Chem. 2010 , 131 , 212 . – reference: T. Furuya , A. S. Kamlet , T. Ritter , Nature 2011 , 473 , 470 . – reference: M. A. McClinton , D. A. McClinton , Tetrahedron 1992 , 48 , 6555 . – reference: V. V. Grushin , W. J. Marshall , J. Am. Chem. Soc. 2006 , 128 , 12644 . – reference: N. D. Ball , J. B. Gary , Y. Ye , M. S. Sanford , J. Am. Chem. Soc. 2011 , 133 , 7577 . – reference: V. C. R. McLoughlin , J. Thrower , Tetrahedron 1969 , 25 , 5921 . – reference: K. Müller , C. Faeh , F. Diederich , Science 2007 , 317 , 1881 . – reference: D. G. Hall , Boronic Acids, Wiley-VCH, Weinheim, Germany, 2005 . – reference: M. Oishi , H. Kondo , H. Amii , Chem. Commun. 2009 , 1909 . – reference: C.-P. Zhang , J. Cai , C.-B. Zhou , X.-P. Wang , X. Zheng , Y.-C. Gu , J.-C. Xiao , Chem. Commun. 2011 , 47 , 9516 . – reference: T. Liu , X. Shao , Y. Wu , Q. Shen , Angew. Chem. Int. Ed. 2012 , 51 , 540 . – reference: G. K. S. Prakash, J. Hu , Acc. Chem. Res. 2007 , 40 , 921 . – reference: J. P. Bégué , D. Bonnet-Delpon , Bioorganic and Medicinal Chemistry of Fluorine, Wiley-Interscience, New Jersey, 2008 . – reference: J. Xu , D.-F. Luo , B. Xiao , Z.-J. Liu , T.-J. Gong , Y. Fu , L. Liu , Chem. Commun. 2011 , 47 , 4300 . – volume: 133 start-page: 7577 year: 2011 publication-title: J. Am. Chem. Soc. – volume: 108 start-page: 14411 year: 2011 publication-title: Proc. Natl. Acad. Sci. USA – volume: 32 start-page: 91 year: 1991 publication-title: Tetrahedron Lett. – year: 2009 – volume: 130 start-page: 8600 year: 2008 publication-title: J. Am. Chem. Soc. – volume: 133 start-page: 20901 year: 2011 publication-title: J. Am. Chem. Soc. – volume: 47 start-page: 4300 year: 2011 publication-title: Chem. Commun. – year: 2005 – volume: 132 start-page: 2878 year: 2010 publication-title: J. Am. Chem. Soc. – volume: 32 start-page: 7689 year: 1991 publication-title: Tetrahedron Lett. – volume: 37 start-page: 320 year: 2008 publication-title: Chem. Soc. Rev. – volume: 6 start-page: 65 year: 2010 publication-title: Beilstein J. Org. Chem. – volume: 66 start-page: 167 year: 1994 publication-title: J. Fluorine Chem. – volume: 128 start-page: 4632 year: 2006 publication-title: J. Am. Chem. Soc. – start-page: 705 year: 1989 publication-title: J. Chem. Soc., Chem. Commun. – volume: 7 start-page: 433 year: 2010 publication-title: Curr. Org. Synth. – volume: 50 start-page: 7655 year: 2011 publication-title: Angew. Chem. Int. Ed. – volume: 128 start-page: 12644 year: 2006 publication-title: J. Am. Chem. Soc. – volume: 133 start-page: 9286 year: 2011 publication-title: J. Am. Chem. Soc. – volume: 76 start-page: 1174 year: 2011 publication-title: J. Org. Chem. – volume: 134 start-page: 9034 year: 2012 publication-title: J. Am. Chem. Soc. – volume: 17 start-page: 6039 year: 2011 publication-title: Chem. Eur. J. – volume: 95 start-page: 2457 year: 1995 end-page: 2483 publication-title: Chem. Rev. – volume: 27 start-page: 6233 year: 2008 publication-title: Organometallics – volume: 133 start-page: 1298 year: 2011 publication-title: J. Am. Chem. Soc. – volume: 131 start-page: 951 year: 2010 publication-title: J. Fluorine Chem. – volume: 61 start-page: 279 year: 1993 publication-title: J. Fluorine Chem. – year: 2008 – year: 2004 – volume: 317 start-page: 1881 year: 2007 publication-title: Science – volume: 11 start-page: 366 year: 1993 publication-title: Chin. J. Chem. – volume: 50 start-page: 1896 year: 2011 publication-title: Angew. Chem. Int. Ed. – volume: 51 start-page: 5947 year: 2010 publication-title: Tetrahedron Lett. – volume: 10 start-page: 4095 year: 1969 publication-title: Tetrahedron Lett. – volume: 108 start-page: 832 year: 1986 publication-title: J. Am. Chem. Soc. – volume: 473 start-page: 470 year: 2011 publication-title: Nature – volume: 67 start-page: 2161 year: 2011 publication-title: Tetrahedron – volume: 12 start-page: 5060 year: 2010 publication-title: Org. Lett. – volume: 55 start-page: 225 year: 1991 publication-title: J. Fluorine Chem. – volume: 48 start-page: 6555 year: 1992 publication-title: Tetrahedron – start-page: 1389 year: 1993 publication-title: J. Chem. Soc., Chem. Commun. – year: 1968 – year: 2003 – volume: 47 start-page: 9516 year: 2011 publication-title: Chem. Commun. – volume: 111 start-page: 4475 year: 2011 publication-title: Chem. Rev. – volume: 17 start-page: 2689 year: 2011 publication-title: Chem. Eur. J. – year: 1996 – volume: 51 start-page: 5048 year: 2012 publication-title: Angew. Chem. Int. Ed. – volume: 328 start-page: 1679 year: 2010 publication-title: Science – volume: 40 start-page: 921 year: 2007 publication-title: Acc. Chem. Res. – volume: 18 start-page: 1577 year: 2012 publication-title: Chem. Eur. J. – volume: 480 start-page: 224 year: 2011 publication-title: Nature – volume: 353 start-page: 1247 year: 2011 publication-title: Adv. Synth. Catal. – volume: 132 start-page: 3648 year: 2010 publication-title: J. Am. Chem. Soc. – volume: 13 start-page: 3596 year: 2011 publication-title: Org. Lett. – volume: 51 start-page: 540 year: 2012 publication-title: Angew. Chem. Int. Ed. – volume: 50 start-page: 3793 year: 2011 publication-title: Angew. Chem. Int. Ed. – volume: 10 start-page: 1719 year: 1981 publication-title: Chem. Lett. – start-page: 932 year: 1980 publication-title: Synthesis – volume: 30 start-page: 3229 year: 2011 publication-title: Organometallics – volume: 41 start-page: 817 year: 2008 publication-title: Acc. Chem. Res. – start-page: 1909 year: 2009 publication-title: Chem. Commun. – volume: 7 start-page: 403 year: 2010 publication-title: Curr. Org. Synth. – volume: 77 start-page: 1251 year: 2012 publication-title: J. Org. Chem. – volume: 133 start-page: 67 year: 2012 publication-title: J. Fluorine Chem. – volume: 25 start-page: 5921 year: 1969 publication-title: Tetrahedron – year: 2006 – volume: 51 start-page: 536 year: 2012 publication-title: Angew. Chem. Int. Ed. – volume: 107 start-page: 5014 year: 1985 publication-title: J. Am. Chem. Soc. – volume: 13 start-page: 2342 year: 2011 publication-title: Org. Lett. – start-page: 1713 year: 2011 publication-title: Synlett – volume: 49 start-page: 9322 year: 2010 publication-title: Angew. Chem. Int. Ed. – volume: 131 start-page: 212 year: 2010 publication-title: J. Fluorine Chem. – volume: 13 start-page: 2479 year: 2012 publication-title: Eur. J. Org. Chem. – ident: e_1_2_7_32_2 doi: 10.1016/S0022-1139(00)80126-8 – ident: e_1_2_7_16_2 doi: 10.1126/science.1190524 – ident: e_1_2_7_81_2 doi: 10.1021/ja200314m – ident: e_1_2_7_41_2 – ident: e_1_2_7_49_2 doi: 10.2174/157017910792246081 – ident: e_1_2_7_50_2 doi: 10.2174/157017910792246117 – ident: e_1_2_7_74_2 doi: 10.1002/anie.201106668 – ident: e_1_2_7_17_2 doi: 10.1021/ja909522s – ident: e_1_2_7_38_2 – ident: e_1_2_7_71_2 doi: 10.1021/jo202566h – ident: e_1_2_7_72_2 doi: 10.1021/jo1023377 – volume-title: Aromatic Fluorination year: 1996 ident: e_1_2_7_2_2 – ident: e_1_2_7_64_2 doi: 10.1021/ja2041942 – ident: e_1_2_7_70_2 doi: 10.1021/ol1023135 – volume-title: Chemistry of Organocopper Compounds year: 2009 ident: e_1_2_7_44_2 – ident: e_1_2_7_4_2 doi: 10.1002/9780470281895 – ident: e_1_2_7_11_2 doi: 10.1038/nature10647 – ident: e_1_2_7_9_2 – ident: e_1_2_7_62_2 doi: 10.1002/adsc.201000825 – ident: e_1_2_7_51_2 doi: 10.1021/ar7002573 – volume-title: Palladium Reagents and Catalysts: New Perspectives for the 21st Century year: 2003 ident: e_1_2_7_68_2 – ident: e_1_2_7_36_2 doi: 10.1039/C39930001389 – ident: e_1_2_7_19_2 doi: 10.1021/ja201726q – ident: e_1_2_7_77_2 doi: 10.1039/c1cc13460d – ident: e_1_2_7_10_2 doi: 10.1073/pnas.1109059108 – ident: e_1_2_7_59_2 doi: 10.1021/om200204y – ident: e_1_2_7_14_2 doi: 10.1021/ja064935c – ident: e_1_2_7_28_2 doi: 10.1016/j.jfluchem.2009.10.011 – volume: 11 start-page: 366 year: 1993 ident: e_1_2_7_31_2 publication-title: Chin. J. Chem. doi: 10.1002/cjoc.19930110411 – ident: e_1_2_7_30_2 doi: 10.1039/c39890000705 – ident: e_1_2_7_42_2 doi: 10.1002/9780470988589 – volume: 40 start-page: 921 year: 2007 ident: e_1_2_7_52_2 publication-title: Acc. Chem. Res. doi: 10.1021/ar700149s – ident: e_1_2_7_40_2 doi: 10.1055/s-0030-1260930 – ident: e_1_2_7_34_2 doi: 10.1016/S0022-1139(00)80112-8 – ident: e_1_2_7_66_2 doi: 10.1002/3527606548 – ident: e_1_2_7_69_2 doi: 10.1021/cr00039a007 – ident: e_1_2_7_57_2 doi: 10.1021/om800794m – volume-title: Suzuki Coupling Reactions year: 2005 ident: e_1_2_7_67_2 – ident: e_1_2_7_75_2 doi: 10.1021/ol2005903 – ident: e_1_2_7_21_2 – ident: e_1_2_7_80_2 doi: 10.1016/j.tetlet.2010.09.027 – ident: e_1_2_7_8_2 doi: 10.1016/j.jfluchem.2010.06.020 – ident: e_1_2_7_33_2 doi: 10.1016/S0040-4039(00)74267-5 – ident: e_1_2_7_13_2 doi: 10.1021/ja0602389 – ident: e_1_2_7_61_2 doi: 10.1039/b823249k – ident: e_1_2_7_48_2 doi: 10.1016/j.tet.2011.01.002 – ident: e_1_2_7_29_2 doi: 10.1246/cl.1981.1719 – ident: e_1_2_7_56_2 doi: 10.1021/ja802946s – ident: e_1_2_7_60_2 doi: 10.1002/anie.201101577 – ident: e_1_2_7_6_2 – ident: e_1_2_7_25_2 doi: 10.1055/s-1980-29276 – ident: e_1_2_7_55_2 doi: 10.1021/ja2081026 – ident: e_1_2_7_1_2 doi: 10.1016/S0040-4020(01)80011-9 – ident: e_1_2_7_43_2 doi: 10.1002/352760393X – ident: e_1_2_7_65_2 – ident: e_1_2_7_79_2 doi: 10.1021/ja301553c – ident: e_1_2_7_12_2 – ident: e_1_2_7_54_2 doi: 10.1002/anie.201006823 – ident: e_1_2_7_18_2 doi: 10.1021/ja100955x – ident: e_1_2_7_37_2 doi: 10.1016/S0040-4039(00)71226-3 – ident: e_1_2_7_46_2 doi: 10.1038/nature10108 – ident: e_1_2_7_3_2 doi: 10.1126/science.1131943 – ident: e_1_2_7_20_2 doi: 10.1002/chem.201100283 – ident: e_1_2_7_24_2 doi: 10.1016/S0040-4039(01)88624-X – ident: e_1_2_7_73_2 doi: 10.1002/chem.201102652 – ident: e_1_2_7_26_2 doi: 10.1021/ja00303a042 – ident: e_1_2_7_58_2 doi: 10.1002/anie.201100633 – ident: e_1_2_7_22_2 – ident: e_1_2_7_23_2 doi: 10.1016/S0040-4020(01)83100-8 – ident: e_1_2_7_7_2 doi: 10.3762/bjoc.6.65 – ident: e_1_2_7_82_2 doi: 10.1002/anie.201106673 – ident: e_1_2_7_45_2 doi: 10.1021/cr1004293 – ident: e_1_2_7_63_2 doi: 10.1002/chem.201002749 – ident: e_1_2_7_76_2 doi: 10.1039/c1cc10359h – ident: e_1_2_7_35_2 doi: 10.1016/0022-1139(93)03014-D – ident: e_1_2_7_39_2 doi: 10.1016/j.jfluchem.2011.07.025 – ident: e_1_2_7_5_2 doi: 10.1039/B610213C – ident: e_1_2_7_15_2 doi: 10.1002/anie.201004051 – ident: e_1_2_7_27_2 doi: 10.1021/ja00264a043 – ident: e_1_2_7_47_2 doi: 10.1002/ejoc.201101535 – ident: e_1_2_7_53_2 doi: 10.1002/anie.201201012 – ident: e_1_2_7_78_2 doi: 10.1021/ol201205t |
| SSID | ssj0009661 |
| Score | 2.4998934 |
| SecondaryResourceType | review_article |
| Snippet | Development of transition‐metal‐catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few... Development of transition-metal-catalyzed trifluoromethylation of arene substrates under mild reaction conditions has attracted great attention in the past few... |
| SourceID | proquest pascalfrancis crossref wiley istex |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 6679 |
| SubjectTerms | Arenes Chemistry Copper Exact sciences and technology Fluorine Noncondensed benzenic compounds Organic chemistry Preparations and properties Trifluoromethylation |
| Title | Progress in Copper-Mediated Formation of Trifluoromethylated Arenes |
| URI | https://api.istex.fr/ark:/67375/WNG-R9PBFJSZ-P/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fejoc.201200648 https://www.proquest.com/docview/1171329937 |
| Volume | 2012 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LT-MwEB4h9gAX3ojwqHJYwSkQp87r2K3aRZWAioeouFi2Y0uFqqn6kBAnfgK_cX_JepwmUKQV0nJLpHEUj2fsb5KZbwB-hopyrWToRZnSHg0k8dLEzzwRyrquR8L4GBYKX1xG53e00wt7H6r4C36I6oMbeobdr9HBuZicvZOGqsccKQgJxsQUq30xYQtR0fU7f5TB8jbionXqGaTSK1kb_eBscfjCqfQDFfyMWZJ8YhSliw4XCxD0I5C1J1F7HXg5hyIB5el0NhWn8uUTveN3JrkBa3OY6jYKu9qEJTXcgpVm2R1uG1pdTOwy26TbH7rNfDRS4z-vbxe28YfK3HZZE-nm2r0d9_VgliMxgjGLgRVoIJXmZAfu2q3b5rk3b8ngSRoSszXGKuY0TqNYKEV0lKiUJOYQRJzh8zCI_SziRESBNpG1zyVNNUmlNpNRGc-IqO_C8jAfqj1wAyMdS6K5_bOZxEmamefKhIpMI4u9A165JEzO-cqxbcaAFUzLAUPlsEo5DpxU8qOCqeOfksd2hSsxPn7C_LY4ZPeXv9l12v3V7tw8sK4DtQUTqAYERjo0wNqBw9Im2Nz3J0ifbkJ8xH0OBHZxv3gf1upcNau7_f8ZdACreF3k2RzC8nQ8U0cGLU1FzXrEX2elC24 |
| linkProvider | Wiley-Blackwell |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LTxsxEB5RONALr7bq8twDak8L6433dYQoIaQkjWhQUS-W7bUlSpSN8pAQJ34Cv5FfgsebXUglVKk97mq8Wo9n7G_s8TcAh6GiXCsZelGmtEcDSbw08TNPhLKma5EwPoYXhTvdqHVF29dhmU2Id2EKfohqww09w87X6OC4IX38whqqfufIQUgwKKbJO1jBst42qrp8YZAyaN7GXLRGPYNVrkveRj84Xmy_sC6toIrvME-ST4yqdFHjYgGEvoaydi1qroMoe1GkoNwezabiSN7_QfD4X93cgLU5UnVPCtPahCU13ILVelkg7gM0epjbZWZK92bo1vPRSI2fHh47tvaHytxmeS3SzbXbH9_owSxHbgRjGQMrcIJsmpOPcNVs9Ostb16VwZM0JGZ2jFXMaZxGsVCK6ChRKUnMOohQw-dhEPtZxImIAm2Ca59LmmqSSm06ozKeEVH7BMvDfKg-gxsY6VgSze3hZhInaWa-KxMqMo1E9g545ZgwOacsx8oZA1aQLQcMlcMq5TjwtZIfFWQdb0p-sUNcifHxLaa4xSH72T1jl2nvtNn-8Yv1HNhfsIGqQWCkQ4OtHdgtjYLN3X-CDOomykfo50BgR_cv_8Ma7e_16mn7XxodwGqr37lgF-fdbzvwHt8XaTe7sDwdz9SeAU9TsW_d4xkczw-J |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LT9tAEB4VkAoXSksrXF4-VO3J4HXWryOEuDQtacRDjXpZrfchUaI4ykNCnPgJ_EZ-SXfWsSFICKk92pqxvLMzu9_Ys98AfAoV5VqJ0Iuk0h4NBPHSxJdeHoqGbkS5iTE8KHzSiY4vaLsX9h6d4i_5IeoPbhgZdr3GAB9Kvf9AGqr-FEhBSDAnpskCLNHIT9Cvj04fCKQMmLcpF21Qz0CVXkXb6Af78_pz29ISWvgayyT52FhKly0u5jDoYyRrt6LsDfBqEGUFytXedJLviZsn_I7_M8o1WJ3hVPegdKy38EoN3sFys2oPtw6tLlZ2mXXSvRy4zWI4VKP727sT2_lDSTerDkW6hXbPR5e6Py2QGcH4Rd8KHCCX5vg9XGSt8-axN-vJ4AkaErM2xirmNE6jOFeK6ChRKUnMLohAw-dhEPsy4iSPAm1Sa58LmmqSCm0GoySXJG98gMVBMVAb4AZGOhZEc_trM4mTVJrnioTmUiONvQNeNSVMzAjLsW9Gn5VUywFD47DaOA58qeWHJVXHs5Kf7QzXYnx0hQVucch-db6y07R7mLXPfrOuAztzLlArBEY6NMjaga3KJ9gs-MfIn25yfAR-DgR2cl94H9Zq_2zWVx__RWkXXnePMvbjW-f7Jqzg7bLmZgsWJ6Op2jbIaZLv2OD4C_gtDkE |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Progress+in+Copper%E2%80%90Mediated+Formation+of+Trifluoromethylated+Arenes&rft.jtitle=European+journal+of+organic+chemistry&rft.au=Liu%2C+Tianfei&rft.au=Shen%2C+Qilong&rft.date=2012-12-01&rft.pub=WILEY%E2%80%90VCH+Verlag&rft.issn=1434-193X&rft.eissn=1099-0690&rft.volume=2012&rft.issue=34&rft.spage=6679&rft.epage=6687&rft_id=info:doi/10.1002%2Fejoc.201200648&rft.externalDBID=10.1002%252Fejoc.201200648&rft.externalDocID=EJOC201200648 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1434-193X&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1434-193X&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1434-193X&client=summon |