Pharmakologisch aktive Polymere, 12. Depotformen von Chlorambucil durch kovalente Bindung an Polymere

Franzmann, Giselher; Ringsdorf, Helmut

doi:10.1002/macp.1976.021770823

Cited by 19 publications

(2 citation statements)

References 7 publications

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“…Thus, the corresponding polyvinylamines can be obtained by indirect routes [15]. For instance, polyvinylamine is prepared by acid or base hydrolysis of the pendant formamide moiety of poly(N-vinylformamide).…”

Section: Other Polyvinylaminesmentioning

confidence: 99%

Vinyl Polymers

Oda¹,

Shinke²

2014

Encyclopedia of Polymeric Nanomaterials

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Section: Other Polyvinylaminesmentioning

confidence: 99%

Vinyl Polymers

Oda¹,

Shinke²

2014

Encyclopedia of Polymeric Nanomaterials

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“…It is used as additive, e.g., in cosmetics [8], pharmaceutical preparations [9–12] and food industry (additive E 1201) [13]. Monoalkylation reactions of N -VP in α-position via deprotonation by lithium diisopropylamide [14] were carried out to open up access to further potential applications of the corresponding polymers [14–16].…”

Section: Introductionmentioning

confidence: 99%

From N-vinylpyrrolidone anions to modified paraffin-like oligomers via double alkylation with 1,8-dibromooctane: access to covalent networks and oligomeric amines for dye attachment

Obels

Lievenbrück

Ritter

2016

Beilstein J. Org. Chem.

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SummaryThe double alkylation of N-vinylpyrrolidone (N-VP) with 1,8-dibromooctane yields paraffin-like oligomeric chains bearing polymerizable vinyl moieties. These oligomers were radically crosslinked in bulk with N-VP as co-monomer yielding swellable polymer disks. The vinylic side groups of the N-VP oligomers allow thiol–ene click reactions with 2-aminoethanethiol hydrochloride to obtain reactive amino-functionalized oligomers. Further modification of the free amino groups with 1,4-difluoro-9,10-anthraquinone (DFA) yields red-colored oligomeric anthraquinone dyes. The final reaction of DFA-substituted N-VP oligomers with Jeffamine® M 600 leads to blue-colored and branched oligomers with poly(ethylene glycol) side chains.

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Polyvinyl Compounds, Others

Hallensleben

2000

Ullmann's Encyclopedia of Industrial Chemistry

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The article contains sections titled: 1. Poly(Vinyl Alcohol) 1.1. Structure and Crystallinity 1.2. Production 1.3. Properties 1.4. Uses, Toxicology, and Economic Aspects 2. Poly(Vinyl Acetals) 2.1. General Aspects 2.2. Poly(Vinyl Formal) 2.3. Poly(Vinyl Butyral) 2.4. Other Poly(Vinyl Acetals) 3. Poly(N‐Vinyllactams) and Poly(N‐Vinylamines) 3.1. Polyvinylpyrrolidone 3.2. Polymers of other N ‐Vinyllactams 3.3. Polyvinylamines

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Pharmakologisch aktive Polymere, 12. Depotformen von Chlorambucil durch kovalente Bindung an Polymere

Cited by 19 publications

References 7 publications

Vinyl Polymers

Vinyl Polymers

From N-vinylpyrrolidone anions to modified paraffin-like oligomers via double alkylation with 1,8-dibromooctane: access to covalent networks and oligomeric amines for dye attachment

Polyvinyl Compounds, Others

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