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
  • [31] Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Chlorobenzenesulfonates
    Bisz, Elwira
    MOLECULES, 2021, 26 (19):
  • [32] Iron-Catalyzed Cross-Coupling Reaction of Alkyl Halides with Biphenyl Grignard Reagent
    Dai, Z. Q.
    Liu, K. Q.
    Zhang, Z. Y.
    Wei, B. M.
    Guan, J. T.
    ASIAN JOURNAL OF CHEMISTRY, 2013, 25 (11) : 6303 - 6305
  • [33] Silver-catalyzed cross-coupling reactions of alkyl bromides with alkyl or aryl Grignard reagents
    Someya, Hidenori
    Yorimitsu, Hideki
    Oshima, Koichiro
    TETRAHEDRON LETTERS, 2009, 50 (26) : 3270 - 3272
  • [34] Iron-Catalyzed Cross-Coupling of Secondary Alkyl Chloride and the Alkynes Grignard Reagent
    Jia, Wan
    Zhao, Lizhi
    Wei, Hengxu
    Zhu, Lindong
    Fu, Lei
    Chen, Weichun
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2016, 36 (05) : 1060 - 1064
  • [35] Vanadium-catalyzed cross-coupling reactions of alkyl halides with aryl grignard reagents
    Yasuda, Shigeo
    Yorimitsu, Hideki
    Oshima, Koichiro
    Bulletin of the Chemical Society of Japan, 2008, 81 (02): : 287 - 290
  • [36] Cobalt-catalyzed Cross-coupling Reactions of Aryl Bromides with Alkyl Grignard Reagents
    Hamaguchi, Hiroyuki
    Uemura, Minoru
    Yasui, Hiroto
    Yorimitsu, Hideki
    Oshima, Koichiro
    CHEMISTRY LETTERS, 2008, 37 (11) : 1178 - 1179
  • [37] Copper-Catalyzed Cross-Coupling of Alkyl and Aryl Grignard Reagents with Alkynyl Halides
    Cahiez, Gerard
    Gager, Olivier
    Buendia, Julien
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (07) : 1278 - 1281
  • [38] Vanadium-catalyzed cross-coupling reactions of alkyl halides with aryl grignard reagents
    Yasuda, Shigeo
    Yorimitsu, Hideki
    Oshima, Koichiro
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2008, 81 (02) : 287 - 290
  • [39] Iron-catalyzed Cross-Coupling of Propargyl Carboxylates and Grignard Reagents: Synthesis of Substituted Allenes
    Kessler, Simon N.
    Backvall, Jan-E.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (11) : 3734 - 3738
  • [40] Gram-Scale, Cheap, and Eco-Friendly Iron-Catalyzed Cross-Coupling between Alkyl Grignard Reagents and Alkenyl or Aryl Halides
    Cahiez, Gerard
    Lefevre, Guillaume
    Moyeux, Alban
    Guerret, Olivier
    Gayon, Eric
    Guillonneau, Loic
    Lefevre, Nicolas
    Gu, Qinzhuo
    Zhou, Edouard
    ORGANIC LETTERS, 2019, 21 (08) : 2679 - 2683