Asymmetric catalysis with heterobimetallic compounds

被引:732
作者
Shibasaki, M
Sasai, H
Arai, T
机构
[1] Grad. Sch. of Pharmaceutical Sci., University of Tokyo, Hongo, Bunkyo-ku
关键词
aluminum; asymmetric catalysis; bimetallic complexes; homogeneous catalysis; lanthanides;
D O I
10.1002/anie.199712361
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This review focuses on a new concept in catalytic asymmetric reactions that was first realized for the use of heterobimetallic complexes. As these heterobimetallic complexes function as both a Brønsted base and as a Lewis acid, just like an enzyme, they make possible a variety of efficient catalytic asymmetric reactions. This heterobimetallic concept should prove to be applicable to a variety of new asymmetric catalyses. The first part of this review describes the development of rare earth-alkali metal complexes such as LnM3tris(binaphthoxide) complexes (LnMB, Ln = rare-earth metal, M = alkali metal), which are readily prepared from the corresponding rare-earth trichlorides or rare-earth isopropoxides, and their application to catalytic asymmetric synthesis. By using a catalytic amount of LnMB complexes several asymmetric reactions proceed efficiently to give the corresponding desired products in up to 98% ee: LnLB-catalyzed asymmetric nitroaldol reactions (L = Li), LnSB-catalyzed asymmetric Michael reactions (S = Na), and LnPB-catalyzed asymmetric hydrophosphonylations of either imines or aldehydes (P = K). Applications of these heterobimetallic catalysts to the syntheses of several biologically and medicinally important compounds are also described. Spectral analyses and computational simulations of the asymmetric reactions catalyzed by the heterobimetallic complexes reveal that the two different metals play different roles to enhance the reactivity of both reaction partners and to position them. From mechanistic considerations, a useful activation of the heterobimetallic catalyses was realized by addition of alkali metal reagents. The second part describes the development of another type of heterobimetallic catalysts featuring Group 13 elements such as Al and Ga as the central metal. Among them, the AlLibis(binaphthoxide) complex (ALB) is an effective catalyst for asymmetric Michael reactions, tandem Michael-aldol reactions, and hydrophosphonylation of aldehydes.
引用
收藏
页码:1236 / 1256
页数:21
相关论文
共 145 条
  • [1] PHOSPHONOPEPTIDES AS ANTIBACTERIAL AGENTS - ALAPHOSPHIN AND RELATED PHOSPHONOPEPTIDES
    ALLEN, JG
    ATHERTON, FR
    HALL, MJ
    HASSALL, CH
    HOLMES, SW
    LAMBERT, RW
    NISBET, LJ
    RINGROSE, PS
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1979, 15 (05) : 684 - 695
  • [2] ANDREWS KJ, 1981, Patent No. 33919
  • [3] [Anonymous], ASYMMETRIC SYNTHESIS
  • [4] AOKI S, 1992, HETEROCYCLES, V33, P493
  • [5] SIMPLE CHIRAL CROWN ETHERS COMPLEXED WITH POTASSIUM TERT-BUTOXIDE AS EFFICIENT CATALYSTS FOR ASYMMETRIC MICHAEL ADDITIONS
    AOKI, S
    SASAKI, S
    KOGA, K
    [J]. TETRAHEDRON LETTERS, 1989, 30 (51) : 7229 - 7230
  • [6] Self-assembly of heterobimetallic complexes and reactive nucleophiles: A general strategy for the activation of asymmetric reactions promoted by heterobimetallic catalysts
    Arai, T
    Yamada, YMA
    Yamamoto, N
    Sasai, H
    Shibasaki, M
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 1996, 2 (11) : 1368 - 1372
  • [7] A new multifunctional heterobimetallic asymmetric catalyst for Michael additions and tandem Michael-Aldol reactions
    Arai, T
    Sasai, H
    Aoe, K
    Okamura, K
    Date, T
    Shibasaki, M
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1996, 35 (01): : 104 - 106
  • [8] Catalytic asymmetric synthesis of alpha-hydroxy phosphonates using the Al-Li-BINOL complex
    Arai, T
    Bougauchi, M
    Sasai, H
    Shibasaki, M
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (09) : 2926 - 2927
  • [9] ARAI T, 1996, ANGEW CHEM, V108, P103
  • [10] PHOSPHONOPEPTIDES AS ANTIBACTERIAL AGENTS - MECHANISM OF ACTION OF ALAPHOSPHIN
    ATHERTON, FR
    HALL, MJ
    HASSALL, CH
    LAMBERT, RW
    LLOYD, WJ
    RINGROSE, PS
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1979, 15 (05) : 696 - 705