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  • Homogeneous catalysis  (1)
  • Keywords. Iridium; Asymmetric Catalysis; Hydroarylation; Hydroamination; Norbornene.  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Monatshefte für Chemie 131 (2000), S. 1345-1350 
    ISSN: 1434-4475
    Schlagwort(e): Keywords. Iridium; Asymmetric Catalysis; Hydroarylation; Hydroamination; Norbornene.
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Summary.  Starting from the dinuclear chloro-bridged Ir(I) complexes [IrCl(PP)]2 (PP = (R)-(6,6′-dimethylbiphenyl-2,2′-diyl)-1,1′-bis-(diphenylphosphine), (R)-(6,6′-dimethoxy-biphenyl-2,2′-diyl)-1,1′-bis-(diphenylphosphine), and (R)-1-((S)-2-(diphenylphosphino-ferrocenyl))-ethyldicyclohexylphosphine), a new class of cyclopentadienyl Ir(I) complexes containing a chiral bisphosphine ([IrCp(PP)]) was prepared and characterized. These new complexes are suited precatalysts for the direct hydroarylation of norbornene with benzamide. 2-(exo-Norbornyl)-benzamide is formed with an enantiomeric excess of up to 94% by the use of 1 mol% iridium, albeit in low yield.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 33 (1994), S. 497-526 
    ISSN: 0570-0833
    Schlagwort(e): N ligands ; Ligand design ; Homogeneous catalysis ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Homogeneous catalysis has been responsible for many major recent developments in synthetic organic chemistry. The combined use of organometallic and coordination chemistry has produced a number of new and powerful synthetic methods for important classes of compounds in general and for optically active substances in particular. For this purpose, complexes with optically active ligands have been used, most of them coordinating through phosphorus. More recent developments have highlighted the use of “nitrogen-donors”, particularly as they are easily obtained from the “chiral pool”. However, the remarkable achievements in this area have been based on an empirical approach. This article attempts to bridge the gap between the synthetic and the coordination chemist. The first section discusses the rates of formation and dissociation of complexes with nitrogen donors, their relationship to the rates of product formation, and presents the factors which induce homolytic cleavage of M—C bonds. It also provides a summary of the main types of organometallic complexes formed by metal centers coordinated to nitrogen donors and their reactivity patterns. The second section highlights the most significant, homogeneously catalyzed reactions involving complexes with nitrogen ligands. Foremost among them are the asymmetric aspects of hydrogenation (particularly those involving boranes as reducing agents), hydrosilylation, cyclopropanations, Diels-Alder reactions, aldol condensations, alkylation of aldehydes, conjugate addition reactions, Grignard cross-coupling reactions, allylic alkylations, oxidation reactions, olefin epoxidations, and di-hydroxylation of olefins.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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