(Q57778132)

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Poly(ether amide) Dendrimers via Nucleophilic Ring-Opening Addition Reactions of Phenol Groups toward Oxazolines: Synthesis and Characterization

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title

Poly(ether amide) Dendrimers via Nucleophilic Ring-Opening Addition Reactions of Phenol Groups toward Oxazolines: Synthesis and Characterization (English)

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2

Brigitte Voit

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Hartmut Komber

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3

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Hartmut Komber

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Dieter Voigt

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4

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Dieter Voigt

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Carola Clausnitzer

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1

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Carola Clausnitzer

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publication date

September 2003

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published in

Macromolecules

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volume

36

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issue

19

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page(s)

7065-7074

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cites work

1H and13C NMR Spectra of a Hyperbranched Aromatic Polyamide from p-Phenylenediamine and Trimesic Acid

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Polymerization of Oxazolines

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Synthesis and Characterization of Poly(ether amide) Dendrimers Containing Different Core Molecules

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Regulation of in vitro gene expression using antisense oligonucleotides or antisense expression plasmids transfected using starburst PAMAM dendrimers

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Hyperbranched Poly(Ether Amide)s via Nucleophilic Ring Opening Reaction of Oxazolines

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New hyperbranched poly(ether amide)s via nucleophilic ring opening of 2‐oxazoline‐containing monomers

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Blends of hyperbranched poly(ether amide)s and polyamide-6

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Synthesis and thermal polymerization of aromatic 2-oxazolines containing carboxylic groups

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Structure characterization of hyperbranched poly(ether amide)s: I. Preparative fractionation

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Hyperbranched Aramids by the A2 + B3 versus AB2 Approach: Influence of the Reaction Conditions on Structural Development

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On Blends of Polyamide 6 and a Hyperbranched Aramid

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New developments in hyperbranched polymers

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Identifiers

DOI

10.1021/MA034318Y

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(Q57778132)

Poly(ether amide) Dendrimers via Nucleophilic Ring-Opening Addition Reactions of Phenol Groups toward Oxazolines: Synthesis and Characterization

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