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  • 1
    ISSN: 0947-6539
    Keywords: heterobimetallic catalysts ; Michael additions ; multifunctional catalysts ; nitroaldol reactions ; self-assembly ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heterobimetallic asymmetric catalysts, such as the lanthanum-lithium-binaphthol complex (La Li-BINOL), the aluminum-lithium-binaphthol complex (AlLi-BINOL), and a newly prepared gallium-sodium-binaphthol complex (Ga Na-BINOL), have been self-assembled with reactive nucleophiles, such as lithium nitronates and sodium malonates, to generate more efficient catalysts than the parent heterobimetallic catalysts. For example, by the combined use of La Li-BINOL (1 mol%; contains one H2O molecule) and BuLi (0.9 mol%) as the catalyst system, asymmetric nitroaldol reactions are greatly accelerated in all cases without a decrease in the optical purity of the nitroaldol products. Kinetic analyses have also been carried out on the Ga Na-BINOL-catalyzed Michael reaction of dibenzyl malonate with cyclohexenone, with or without NaOtBu. The calculated rate constants show that the combined use of Ga Na-BINOL and NaOtBu as the catalyst gives reaction rates that are about 50 times faster than with Ga Na-BINOL alone. This activation method should be useful for other asymmetric reactions catalyzed by heterobimetallic complexes.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 109 (1997), S. 1942-1944 
    ISSN: 0044-8249
    Keywords: Aldolreaktionen ; Asymmetrische Katalyse ; Asymmetrische Synthese ; Homogene Katalyse ; Lanthan ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-8249
    Keywords: Aldolreaktionen ; Aluminiumverbindungen ; Kaskadenreaktionen ; Katalyse ; Michael-Additionen ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 109 (1997), S. 1290-1311 
    ISSN: 0044-8249
    Keywords: Aluminium ; Asymmetrische Katalyse ; Homogene Katalyse ; Lanthanoide ; Zweikernkomplexe ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Im Mittelpunkt dieser Übersicht steht ein neues Katalyseprinzip in asymmetrischen Reaktionen, das erstmals durch die Verwendung von Hetero-Dimetall-Komplexen verwirklicht wurde, die wie ein Enzym sowohl Brønsted-basische als auch Lewis-saure Eigenschaften aufweisen und so eine effiziente Katalyse vieler asymmetrischer Reaktionen ermöglichen. Dieses Prinzip sollte sich auf viele neue asymmetrische Katalysen übertragen lassen. Im ersten Teil dieser Übersicht beschreiben wir die Entwicklung und die Anwendung von Seltenerdmetall-Alkalimetall-Komplexen wie LnM3-Tris(binaphthyloxid) (LnMB; Ln = Seltenerdmetall, M = Alkalimetall) in der katalytischen asymmetrischen Synthese. In Gegenwart katalytischer Mengen an den LnMB-Komplexen, die leicht aus den entsprechenden Trichloriden und/oder Isopropoxiden der Seltenerdmetalle zugänglich sind, verlaufen viele asymmetrische Reaktionen effizient und mit bis zu 98% Enantioselektivität: LnLB-katalysierte asymmetrische Nitroaldolreaktionen (L = Li), LnSB-katalysierte asymmetrische Michael-Additionen (S = Na) und LnPB-katalysierte asymmetrische Hydrophosphonylierungen von Iminen und Aldehyden (P = K). Die Anwendung dieser Hetero-Dimetall-Katalysatoren in der Synthese einiger biologisch und medizinisch bedeutender Verbindungen wird beschrieben. Spektroskopische Untersuchungen und Computersimulationen der Hetero-Dimetall-Komplex-katalysierten asymmetrischen Reaktionen deuten darauf hin, daß zwei unterschiedliche Metalle verschiedene Aufgaben bei der Reaktivitätssteigerung und Ausrichtung der beiden Reaktionspartner übernehmen. Aufgrund mechanistischer Überlegungen wurden Alkalimetallreagentien zugesetzt, die zur Aktivierung der Hetero-Dimetall-Katalysatoren führten. Im zweiten Teil dieser Übersicht gehen wir auf die Entwicklung von Hetero-Dimetall-Katalysatoren mit Elementen der 13. Gruppe, wie Al und Ga, als Zentralmetall ein. Der Al-Li-Bis(binaphthyloxid)-Komplex (ALB) erwies sich dabei als leistungsfähiger Katalysator für asymmetrische Michael-Additionen, Tandem-Michael-Aldol-Reaktionen und die Hydrophosphonylierung von Aldehyden.
    Additional Material: 8 Ill.
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  • 5
    ISSN: 0570-0833
    Keywords: aldol reactions ; aluminum compounds ; cascade reactions ; catalysis ; Michael additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 36 (1997), S. 1236-1256 
    ISSN: 0570-0833
    Keywords: aluminum ; asymmetric catalysis ; bimetallic complexes ; homogeneous catalysis ; lanthanides ; Aluminum ; Asymmetric catalysis ; Dimetallic complexes ; Homogeneous catalysis ; Lanthanides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 36 (1997), S. 1871-1873 
    ISSN: 0570-0833
    Keywords: aldol reactions ; asymmetric catalysis ; asymmetric synthesis ; homogeneous catalysis ; lanthanum ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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