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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1321-1325 
    ISSN: 0009-2940
    Keywords: Arene Complexes ; Ruthenium ; Diastereoselective ; Reduction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two preparative routes are reported that give access to the racemic series of planar chiral [(arene)(COD)Ru] derivatives containing η6-bonded o-tolyl ketone or aldehyde arene units. The ketone and aldehyde functions of these have subsequently been reduced by nBuLi and PhLi, respectively. Hydrolysis converts the initially formed lithium salts into diastereomeric benzyl alcohol complexes lithium salts into diastereomeric benzyl alcohol complexes in high yields. The formation of the new stereogenic centre is diastereoselective (88% de) for the aldehyde and diastereospecific for the ketone (de 〉 99%). Due to a sterically overcrowded situation, the rotation of the chiral side chain of [(COD) (η6-o-tolyl-tert-butylphenylmethanol) Ru] (7) is hindered, as is the rotation of the phenyl and tert-butyl substituents. As a consequence, the hydroxyl group is fixed at a position close to the metal both in solution and in the solid state.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0570-0833
    Keywords: Arene ligands ; Intermediates ; Cocondensation ; Sandwich complexes ; Synthetic methods ; Iron ; Metal atoms ; Cobalt ; Nickel ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In 1969, P. L. Timms reported the first preparative cocondensation reactions of metal vapors with organic and inorganic substrates. The use of this technique in preparative chemistry soon spread rapidly, but in recent years there has been less activity in this sector. If metal atom reactions are not utilized primarily for the formation of new products, but for the synthesis of highly reactive intermediates, a new synthetic strategy may be developed. Our aims are reaction sequences which, based on an effective cocondensation reaction, lead gradually and selectively to new substance classes. This principle can be illustrated by the example of the cocondensation products of arenes and iron, cobalt, or nickel vapor, which decompose between -70 and -50°C. The classes of products accessible by this method extend from clusters, through π-complexes, organophosphorus and organoboron cage compounds to pure organic cycloaddition products.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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