Chiral [Bis(olefin)amine]rhodium(I) Complexes - Transfer Hydrogenation in Ethanol

被引:30
|
作者
Zweifel, Theo [1 ]
Scheschkewitz, David [1 ]
Ott, Timo [1 ]
Vogt, Matthias [1 ]
Gruetzmacher, Hansjoerg [1 ]
机构
[1] ETH, Dept Chem & Appl Chem, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Asymmetric catalysis; Enantioselectivity; Ethanol; Olefin complexes; Rhodium; Transfer hydrogenation; ASYMMETRIC TRANSFER HYDROGENATION; LIGANDS; CATALYSTS; DERIVATIVES; REACTIVITY; RHODIUM(I); KETONES; ACIDS;
D O I
10.1002/ejic.200900875
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Bis(olefin)amines (boas) are a new class of ligands for the synthesis of transition metal complexes, which can be used in various homogeneous catalytic reactions. A simple straightforward coupling reaction between 5H-dibenzo[a,d]cyclohepten-5-yl chloride (tropCl) and primary amines allows the synthesis of various chiral boas. Birch reduction of phenylalanine gives (2S)-2-amino-3-cyclohexa-1,4-dien-1-yl propanoate, which is used for the synthesis of the bis(olefin)amine methyl (2S)-3-(cyclohexa-1,4-dienyl)-2-(5H-dibenzo[a,d]cyclohepten-5-yl-amino)propionate. Coupling between cyclohex-3-en-1-ylamine with tropCl gives N-(cyclohex-3'-en-1'-yl)-5H-dibenzo[a,d]cyclohepten-5-ylamine, which was separated into its enantiomers. Bicyclic cyclohexenylamine derivatives like bicyclo[2.2.2]oct-5-en-2-ylamine and 2(methoxycarbonyl)bicyclo(2.2.1]hept-5-en-3-ylamine were likewise coupled with tropCl to give chiral bis(olefin)amines. Alternatively, 5H-dibenzo[a,d]cyclohepten-5-ylamine (trop-NH2) can react with cyclohexenyl ketones to give prochiral bis(olefin)imines, which were reduced to the corresponding bis(olefin)amines. With [Rh-2(mu-Cl)(2)(CO)(4)] or [Rh-2(mu-Cl)(2)(C2H4)(4)], a complexation of these compounds was achieved leading to chiral rhodium complexes of the type [Rh(boa)(CO)]OTf or [Rh(boa)(PR3)]OTf. The complexes have a strongly distorted saw-horse-type structure (determined by X-ray diffraction studies) and were tested in transfer hydrogenations with ethanol/2-propanol as hydrogen donor. Only complexes with tightly bound olefinic binding sites and a pronounced saw-horse-type structure give significant activities. Furthermore, a phosphane ligand in trans position to the coordinated amine function has a positive impact of the catalysts performance. None of the investigated catalysts gave an impressive enantiomeric excess (ee < 60%) in the transfer hydrogenation of acetophenone. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
引用
收藏
页码:5561 / 5576
页数:16
相关论文
共 50 条
  • [31] STEREOCHEMICAL PATTERN OF HOMOGENEOUS HYDROGENATION OF OLEFINIC COMPOUNDS BY RHODIUM(I) COMPLEXES OF A CHIRAL PHOSPHINE
    PAIARO, G
    PANDOLFO, L
    GAZZETTA CHIMICA ITALIANA, 1977, 107 (9-10): : 467 - 472
  • [32] ASYMMETRIC HYDROGENATION USING CHIRAL PHOSPHINITE RHODIUM COMPLEXES
    BAKOS, J
    TOTH, I
    HEIL, B
    TETRAHEDRON LETTERS, 1984, 25 (43) : 4965 - 4966
  • [33] ASYMMETRIC HYDROGENATION BY CHIRAL AMINOPHOSPHINE-RHODIUM COMPLEXES
    FIORINI, M
    GIONGO, GM
    MARCATI, F
    MARCONI, W
    JOURNAL OF MOLECULAR CATALYSIS, 1976, 1 (06): : 451 - 453
  • [34] RHODIUM(I) DERIVATIVES OF HARD LIGANDS AS OLEFIN HYDROGENATION CATALYSTS
    CULLEN, WR
    WICKENHEISER, EB
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1987, 194 : 346 - INOR
  • [35] HYDROGENATION OF CATIONIC BIS(TERTIARY ALKYLPHOSPHINE)RHODIUM(I) COMPLEXES - AN NMR-STUDY
    BUTLER, IR
    CULLEN, WR
    MANN, BE
    NURSE, CR
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1985, 280 (02) : C47 - C50
  • [36] Rhodium(I) bis(aminophosphane) complexes as catalysts for asymmetric hydrogenation of activated ketones.
    Roucoux, A
    Suisse, I
    Devocelle, M
    Carpentier, JF
    Agbossou, F
    Mortreux, A
    TETRAHEDRON-ASYMMETRY, 1996, 7 (02) : 379 - 382
  • [37] Isomerization of aldehydes catalyzed by rhodium(I) olefin complexes
    Lenges, CP
    Brookhart, M
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1999, 38 (23) : 3533 - 3537
  • [38] New chiral cationic rhodium-aminophosphine complexes for asymmetric transfer hydrogenation of aromatic ketones
    Gao, JX
    Yi, XD
    Xu, PP
    Tang, CL
    Wan, HL
    Ikariya, T
    JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1999, 592 (02) : 290 - 295
  • [39] SYNTHESIS AND CHARACTERIZATION OF RHODIUM(I) AMINO OLEFIN COMPLEXES
    KRAFFT, ME
    WILSON, LJ
    ONAN, KD
    ORGANOMETALLICS, 1988, 7 (12) : 2528 - 2534
  • [40] Chiral bis(oxazolinyl)phenyl rhodium and palladium complexes
    Motoyama, Y
    Makihara, N
    Mikami, Y
    Aoki, K
    Nishiyama, H
    CHEMISTRY LETTERS, 1997, (09) : 951 - 952