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  • 1
    Unknown
    Berlin, Heidelberg : Springer
    Keywords: Biochemistry ; Chemistry, Organic ; Nanotechnology ; Polymers
    ISBN: 9783540314745
    Language: English
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 451-458 
    ISSN: 1434-193X
    Keywords: Cross-coupling ; Modular chemistry ; Repetitive synthesis ; Macrocycles ; Shape persistence ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The synthesis of a variety of kinked oligophenylene building blocks is described. The synthetic strategy is repetitive, utilizes the Suzuki cross-coupling protocol, and involves potentially bifunctional building blocks (modules) which carry one functional group for coupling and one group which serves as place holder. After the coupling, the placeholder is converted into a coupling functionality for the next growth step. The building blocks also carry chloro-substituents which are unaffected by all transformations. For one of the large building blocks it is shown that it actually can be cyclized into an oligophenylene macrocycle with a chloro-substituent at each corner and a pair of hexyl chains at each side.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 1275-1283 
    ISSN: 1434-193X
    Keywords: Dendrimers ; Amino-functionalized dendrons ; Building blocks ; Protecting groups, orthogonal ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The multi-gram scale synthesis of first- and second-generation dendrons with Boc- and Cbz-protected amino groups in the periphery and methyl/ethyl esters at the focal points is described. Saponification of the esters and deprotection of the amines are shown to be strictly orthogonal processes which makes these dendrons valuable building blocks for future constructions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 99-105 
    ISSN: 1434-193X
    Keywords: Ladder polymers ; Macrocycles ; Cycloadditions ; Retro Diels-Alder reaction ; Benzo[c]furan ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the AB-type Diels-Alder (DA) monomer 12 is reported whose self-condensation leads to the formation of the linear ladder oligomer 17 and its cyclic congener 18. 18 is the largest [n]cyclacene derivative known (n = 18) and can be obtained by thermal treatment of 17 in yields of up to 45% utilizing the reversibility of the DA cyclization involved. 17 can be considered a “storage form” for 18.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2551-2556 
    ISSN: 1434-193X
    Keywords: Dendrimers ; Hydroxy-functionalized dendrons ; Orthogonal protective groups ; Building blocks ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A convenient and practical multi-gram procedure for the synthesis of second- (G2; 4a, 5a, 5d) and third-generation (G3; 6a) dendrons with orthogonally protected functional groups in the periphery (hydroxy) and at the focal point (carboxylic acid) is described. It uses the amply available first-generation dendrons with amine and carboxylic ester functions (1) and tetrahydropyranyl-protected hydroxy and carboxylic acid functions (2b, 3), respectively, which are connected via amides by peptide methods. Purification is either done by recrystallization or simple filtration through silica gel and yields the products as analytically pure materials on a several-gram scale (even for G3). ‘The dendrons’ protective groups are proven to be orthogonal (500-MHz NMR) which makes them useful components (building blocks) of a future dendron construction kit for a versatile synthesis of, for example, dendronized polymers.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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