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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 1767-1772 
    ISSN: 1434-193X
    Keywords: Circular dichroism ; Conformation analysis ; s-Triazines ; Chiral auxiliaries ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---CD data of the optically pure 2-[(R)-1-(9-anthryl)ethylamino]-4-chloro-6-[(R)-1-(1-naphthyl)ethylamino]-1,3,5-triazine, 2[(R)-1-(9-anthryl)ethylamino]-4,6-bis[(R)-1-(1-naphthyl)ethylamino]-1,3,5-triazine, 2,4-bis[(R)-1-(9-anthryl)ethylamino]-6-chloro-1,3,5-triazine are presented. The analysis of the CD spectra by means of the nonempirical DeVoe approach has afforded the complete conformational characterisation of the three s-triazine derivatives, allowing us to establish how the conformation of these derivatives depends on the nature of the substituent 1-arylethylamino groups.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 1165-1171 
    ISSN: 1434-193X
    Keywords: Porphyrinoids ; Asymmetric catalysis ; Atropisomerism ; Epoxidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -A new series of porphyrins has been synthesised, incorporating four identical chiral binaphthyl derivatives in the meso-positions. Owing to a hindered rotation around the bond between the naphthyl and the porphyrin, four atropisomers are generated, which were fully separated by preparative TLC and thoroughly characterised. The free bases were metallated with iron(III) and manganese(III) and the resulting complexes were used as catalytic precursors in styrene epoxidation. The reactions show chemoselectivity and enantioselectivity, depending on the stereochemistry of the metalloporphyrin. It is demonstrated that highest efficiency is performed by the ααββ isomer, showing C2 symmetry.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-193X
    Keywords: Cyclodextrins ; NMR spectroscopy ; Chiral solvating agent ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Benzoylated and benzylated cyclodextrins give rise to non-equivalence in the 1H-NMR spectra of racemates of 3,5-dinitrophenyl derivatives of chiral amines, amino alcohols, alcohols, carboxylic acids and amino acids in CDCl3 solution, suggesting their potential use as CDCl3-soluble cyclodextrinic chiral solvating agents (CSAs) in NMR spectroscopy. Cyclodextrins bearing aromatic substituents at the primary or secondary sites only are more efficient CSAs compared to exhaustively substituted ones. NMR investigations based on NOE measurements or complexation shift determinations strongly suggest non-inclusive interaction mechanisms for these selector/selectand systems.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 2000 (2000), S. 75-82 
    ISSN: 1434-1948
    Keywords: Macrocyclic ligands ; Conformational equilibria ; EXSY spectroscopy ; Lanthanide-induced shifts ; Solution structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structure and the conformational equilibria in aqueous and methanolic solutions of YbDOTMA (DOTMA = (1R,4R,7R,10R)-α,α′,α′′,α′′′′-tetramethyl-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) are investigated and the dynamics studied by means of NMR methods. The presence of two isomeric forms in slow exchange is confirmed and quantitatively characterized by EXSY. The exchange peaks are assigned to the inversion of the conformation of the macrocycle ring. No evidence is obtained of a reorientation of the methyl acetate substituents. The protons switch between positions with the same geometrical factors, i.e. positions that would have the same pseudocontact shifts were it not for the different magnetic susceptibility anisotropies of the two species; steady-state NOE spectra on the major form allow unequivocal assignment of the conformations of the two isomers.Supporting information for this article is available on the WWW under -//_/_http://www.wiley-vch.de/contents/jc_2005/2000/99141_s.pdf or from the author.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-193X
    Keywords: Cyclodextrins ; NMR spectroscopy ; NOE ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The conformational features of alkylated, benzoylated, and benzylated cyclodextrins in solution were analysed by NOE and proton-selective relaxation methods and were compared to those of native compounds.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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