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  • 1
    ISSN: 0009-2940
    Keywords: Aminocarbene complexes, of chromium and tungsten ; 3-Aza-1-metalla-1,3-dienes, of chromium and tungsten ; 5-Aza-1-metalla-1,3,5-trienes, cyclization to 2H-pyrroles ; 2H-Pyrrole complexes, of chromium and tungsten ; Pyrroles, syntheses by metal-induced [3 + 2] cycloaddition reactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 551). - 5-Aza-1-metalla-1,3,5-trienes of Chromium and Tungsten, and Their Cyclization to 2H-Pyrrole Complexes5-Aza-1-metalla-1,3,5-trienes 5 and 6 [LnM = C - C = C - N = C, a: LnM = Cr(CO)5, b: W(CO)5] are obtained in two steps from aminocarbene complexes 1 [LnM = C(NH2)Ph, a: LnM = Cr(CO)5, b: W(CO)5]. The first step involves the condensation of 1 with benzaldehyde (2) in the prescence of TiCl4/Et3N to give 3-aza-1-metalla-1,3-dienes 3 (LnM = C - N = C). 3 adds to the 1-aminoalkyne 4 to give 5 and 6 by a chain extension of two carbon atoms. The trans isomers 5 are formed as the major products and are stable both in the solid state and in solution. The cis isomers 6 undergo a novel-type cyclization to give 2H-pyrrole complexes 8. Triene 5b was characterized by an X-ray analysis.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2475-2478 
    ISSN: 1434-193X
    Keywords: Anionic polymerization ; Conformational enantiomer ; Hydrogen bonds ; Intimate ion pair ; Carbanions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The treatment of benzylphenylsulfone with tetrabutylammonium hydroxide results in the formation of the title compound tetrabutylammonium phenyl(phenylsulfonyl)methylide. An X-ray structural analysis of the racemate shows the presence of a chiral metal-free carbanion in the form of an intimate ion pair. Stabilization of the conformational enantiomer occurs by a three-point interaction with two of the α-methylene moieties of the tetrabutylammonium ion, CH···O hydrogen bonding being the driving force. The ion pair is capable of initiating the anionic polymerization of acrylates.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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