ArticleOrganic letters2013
Dendrimers terminated with dichlorotriazine groups provide a route to compositional diversity.
Article in Organic letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
4 citing papers in PubMed.
- Solid-Phase Synthesis of Well-Defined Defect Lysine Dendrimers.Methods in molecular biology (Clifton, N.J.) · 2025Article
- Click Chemistry of Melamine Dendrimers: Comparison of "Click-and-Grow" and "Grow-Then-Click" Strategies Using a Divergent Route to Diversity.Molecules (Basel, Switzerland) · 2022Article
- Two Decades of Triazine Dendrimers.Molecules (Basel, Switzerland) · 2021Review
- Nanoparticle Effects on Human Platelets in Vitro: A Comparison between PAMAM and Triazine Dendrimers.Molecules (Basel, Switzerland) · 2016Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
Triazine dendrimers terminated with either four or eight dichlorotriazines can be prepared in high yields by reacting an amine-terminated dendrimer with cyanuric chloride. These materials exist as white powders and are stable to storage at room temperature. Sequential nucleophilic aromatic substitution with two different amine nucleophiles yields compounds that display the desired compositional diversity. Reaction conditions for the substitution were developed using a model dichlorotriazine with amine nucleophiles at -20, 0, and 25 °C. Selective substitution is favored at lower temperatures and with more nucleophilic amine groups.
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Registered trials
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