Chiral lithium salts of phosphoric acids as lewis acid-base conjugate catalysts for the enantioselective cyanosilylation of ketones

被引:102
作者
Hatano, Manabu [1 ]
Ikeno, Takumi [1 ]
Matsumura, Tokihiko [1 ]
Torii, Shinobu [1 ]
Ishihara, Kazuaki [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词
asymmetric catalysis; cyanohydrins; cyanosilylation; ketones; lithium; phosphoric acids;
D O I
10.1002/adsc.200800314
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The catalytic enantioselective cyanosilylation of aromatic ketones was developed by using chiral lithium salts of (R)-BINOL- or (S)-BINAM-derived phosphoric acid compounds. In the presence of 1.0 mol% of chiral conjugate lithium salts, the corresponding tertiary cyanohydrins were obtained in high yields with moderate to high enantioselectivities. This is the first efficient example of asymmetric catalysis using lithium salts of synthetically useful chiral phosphoric acid compounds. A possible catalytic mechanism and transition states are also discussed as a preliminary working hypothesis.
引用
收藏
页码:1776 / 1780
页数:5
相关论文
共 74 条
  • [51] Practical synthesis of chiral ligands for catalytic enantioselective cyanosilylation of ketones
    Masumoto, S
    Yabu, K
    Kanai, M
    Shibasaki, M
    [J]. TETRAHEDRON LETTERS, 2002, 43 (16) : 2919 - 2922
  • [52] NORTH M, 1993, SYNLETT, P807
  • [53] Synthesis and applications of non-racemic cyanohydrins
    North, M
    [J]. TETRAHEDRON-ASYMMETRY, 2003, 14 (02) : 147 - 176
  • [54] Lewis base catalyzed asymmetric reactions involving hypervalent silicate intermediates
    Orito, Y
    Nakajima, M
    [J]. SYNTHESIS-STUTTGART, 2006, (09): : 1391 - 1401
  • [55] Enantioselective cyanosilylation of α,α-dialkoxy ketones catalyzed by proline-derived in-situ-prepared N-oxide as bifunctional organocatalyst
    Qin, Bo
    Liu, Xiaohua
    Shi, Jian
    Zheng, Ke
    Zhao, Haitao
    Feng, Xiaoming
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2007, 72 (07) : 2374 - 2378
  • [56] Hypervalent silicon as a reactive site in selective bond-forming processes
    Rendler, S
    Oestreich, M
    [J]. SYNTHESIS-STUTTGART, 2005, (11): : 1727 - 1747
  • [57] Bronsted acid-catalyzed imine amidation
    Rowland, GB
    Zhang, HL
    Rowland, EB
    Chennamadhavuni, S
    Wang, Y
    Antilla, JC
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (45) : 15696 - 15697
  • [58] Enantioselective Bronsted acid catalyzed transfer hydrogenation: Organocatalytic reduction of imines
    Rueping, M
    Sugiono, E
    Azap, C
    Theissmann, T
    Bolte, M
    [J]. ORGANIC LETTERS, 2005, 7 (17) : 3781 - 3783
  • [59] Enantioselective cyanosilylation of ketones catalyzed by a chiral oxazaborolidinium ion
    Ryu, DH
    Corey, EJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (15) : 5384 - 5387
  • [60] Schiffers R, 1997, SYNLETT, P1175