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  • Lewis acids  (1)
  • N-(4-methoxycarbonylphenyl)imine  (1)
  • Organic Chemistry  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 9 (1995), S. 467-471 
    ISSN: 0268-2605
    Keywords: lanthanum isopropoxide ; imines ; methylmalonitrile ; methyl 2-cyanopropanoate ; α-imino ester ; N-toluenesulfonylimine ; N-(4-methoxycarbonylphenyl)imine ; addition to imines ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The addition of certain activated nucleophiles to activated imines is catalyzed by lanthanum isopropoxide. As activated nucleophiles, methylmalononitrile and methyl 2-cyanopropanoate can be utilized. Imines having an electronwithdrawing group either at the carbon or at the nitrogen atom of the C=N double bond can be used; for example N-toluenesulfonylimines, N-(4-methoxycarbonylphenyl)imines and α-imino esters.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 947-959 
    ISSN: 0570-0833
    Keywords: Lewis acids ; Synthetic methods ; Selectivity ; Organocopper compounds ; Addition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic compounds with pronounced nucleophilicity such as organocopper and organolithium compounds, and powerful electrophiles, such as BF3 and AlCl3, are generally thought to be incompatible under normal, homogeneous reaction conditions. As a matter of course, it is anticipated that the two species cannot coexist and undergo transmetalation reactions. To our surprise, however, RCu and BF3 are compatible at low temperature. RCu·BF3 and related organocopper-Lewis acid reagents exhibit new and unique reactivities and selectivities: in conjugate additions, e.g., not only activation but also high regio-, stereo-, and chemo-selectivity as well as very high asymmetric induction is observed; allylic derivatives are alkylated regioselectively, and reaction towards carbonyl groups, imines, epoxides, aziridines, ethers, acetals, orthoformates, and pyridinium salts is in each case found to be selective. RLi·BF3 and related organolithium-Lewis acid reagents also exhibit noteworthy selectivities and reactivities. These complex reagents are utilized in the key steps of the total synthesis of many important natural products, such as certain terpenes, steroids, and alkaloids.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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