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  • siloxanes  (2)
  • 1995-1999  (2)
  • 1
    ISSN: 0268-2605
    Keywords: siloxanes ; carbohydrate modified ; surfactants ; saccharide ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New siloxanyl-modified carbohydrate surfactants of the amide and glycoside type have been synthesized by coupling between defined as well as higher-molecular-weight siloxanes and carbohydrate structures via spacers of different lengths and hydrophilic power. Linear and branched monohydrogen di-, tri-, tetra- and penta-siloxanes and polyhydrogen siloxanes as well as mono- and di-saccharide lactone structures have been found to be good starting materials for the synthesis of amides, often in quantitative yield, whereas glycosides had to be prepared in low-yield multistep sequences including protection/deprotection steps. Selected strategies were applied to polysiloxanes yielding quantitatively a broad variety of carbohydrate-modified comb-like structures. The new substances were characterized by means of 13C NMR spectroscopy, GC, capillary GC, GC-MS coupling and elemental analysis.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 10 (1996), S. 437-450 
    ISSN: 0268-2605
    Keywords: siloxanes ; surfactant ; carbohydrate ; amino ; regioselective ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Branched siloxanyl-modified carbohydrate surfactants have been synthesized by coupling mono-, di- and poly-functional siloxanes to carbohydrate units either via a branched spacer or by attaching a separate modifying element to a straight-chained structure. Hydrophilic as well as extremely hydrophobic elements have been incorporated successfully. Siloxanyl-modified carbohydrates bearing a secondary amino function were alkylated in regioselective reactions by different epoxides ranging from glycidol- to siloxanyl-modified allyl glycidyl ether derivatives. Alternatively, carbohydrate-modified piperazinyl structures yielded cyclic subunits after alkylation. Structures bearing two identical hydrophilic groups are accessible by alkylation of carbohydrate-modified bisamides. The derivatives synthesized were characterized by means of GC, NMR and elemental analysis.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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