Low Temperature Studies of Iron-Catalyzed Cross-Coupling of Alkyl Grignard Reagents with Aryl Electrophiles

被引:39
|
作者
Kleimark, Jonatan [1 ]
Larsson, Per-Fredrik [1 ]
Emamy, Parisa [1 ]
Hedstrom, Anna [1 ]
Norrby, Per-Ola [1 ]
机构
[1] Univ Gothenburg, Dept Chem, SE-41296 Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
cross-coupling; density functional calculations; iron; kinetics; reaction mechanism; ALKENYL HALIDES; MECHANISMS; COMPLEXES; ARYLATION; PHOSPHINE; ENERGIES;
D O I
10.1002/adsc.201100392
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The title reaction has been studied under low temperature conditions. Coupling with active substrates can be done even at dry ice temperature. Initial rate studies at -25 degrees C indicate that high concentrations of any reagent can lead to either complete or partial catalyst deactivation. Under strongly reducing conditions, iron seems to form less active complexes that only slowly re-enter the catalytic cycle, possibly through bimolecular coupling of iron(II) complexes. Computational studies support the experimental observations, and indicate that oxidation states below +I cannot be reached by reductive elimination.
引用
收藏
页码:448 / 456
页数:9
相关论文
共 50 条
  • [1] Iron-catalyzed cross-coupling of heteroaromatic tosylates with alkyl and aryl Grignard reagents
    Chen, Xu
    Quan, Zheng-Jun
    Wang, Xi-Cun
    [J]. APPLIED ORGANOMETALLIC CHEMISTRY, 2015, 29 (05) : 296 - 300
  • [2] Iron-catalyzed cross-coupling of primary and secondary alkyl halides with aryl Grignard reagents
    Nakamura, M
    Matsuo, K
    Ito, S
    Nakamura, E
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (12) : 3686 - 3687
  • [3] Iron-catalyzed cross-coupling of aryltrimethylammonium triflates and alkyl Grignard reagents
    Guo, Wang-Jun
    Wang, Zhong-Xia
    [J]. TETRAHEDRON, 2013, 69 (46) : 9580 - 9585
  • [4] Iron-catalyzed cross-coupling of alkyl halides with alkenyl grignard reagents
    Guerinot, Amandine
    Reymond, Sebastien
    Cossy, Janine
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (34) : 6521 - 6524
  • [5] Iron-catalyzed coupling of aryl grignard reagents with alkyl halides
    Hedstrom, Anna
    Norrby, Per-Ola
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [6] Schlenk equilibrium effects on iron-catalyzed cross-coupling reactions of aryl chlorides with alkyl Grignard reagents
    Perry, Marc C.
    Gillett, Amber N.
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [7] Iron-catalyzed cross-coupling reactions of alkyl-grignard reagents with aryl chlorides, tosylates, and triflates
    Fürstner, A
    Leitner, A
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2002, 41 (04) : 609 - +
  • [8] Iron-Catalyzed Cross-Coupling of Diarylzinc or Aryl Grignard Reagents with Difluoroalkyl Bromides
    An Lun
    Tong Feifei
    Zhang Xingang
    [J]. ACTA CHIMICA SINICA, 2018, 76 (12) : 977 - 982
  • [9] Iron-Catalyzed Enantioselective Cross-Coupling Reactions of α-Chloroesters with Aryl Grignard Reagents
    Jin, Masayoshi
    Adak, Laksmikanta
    Nakamura, Masaharu
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (22) : 7128 - 7134
  • [10] Iron-Catalyzed Cross-Coupling of Unactivated Secondary Alkyl Thio Ethers and Sulfones with Aryl Grignard Reagents
    Denmark, Scott E.
    Cresswell, Alexander J.
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2013, 78 (24): : 12593 - 12628