Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 270

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Combining ATRP and “Click” Chemistry: a Promising Platform toward Functional Biocompatible Polymers and Polymer Bioconjugates

Lutz, Jean-François, Börner, Hans G., Weichenhan, Katja·2006·Macromolecules

Abstract

The bromine chain-ends of well-defined poly(oligo(ethylene glycol) acrylate) (POEGA) ( M n = 6850 g·mol -1, M w / M n = 1.21) prepared using ATRP were successfully transformed into various functional end groups (ω-hydroxy, ω-amino, and ω-Fmoc-amino acid) via a two step pathway: (1) substitution of the bromine terminal atom by an azide function, (2) 1,3-dipolar cycloaddition of the terminal azide and functional alkynes (propargyl alcohol, propargylamine, and N -α-(9-fluorenylmethyloxycarbonyl)- l -propargylglycine). The efficient “click” cycloaddition was confirmed in all cases by 1 H NMR or SEC−UV analysis. Moreover, this two-step synthetic strategy was also studied for preparing polymer- b -oligopeptide bioconjugates. Well-defined POEGA- b -GGRGDG was obtained in high yields via the “click” ligation of the azido functional POEGA and the alkyne functional oligopeptide GGRGDG.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1021/ma061557n

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 2 references

Cited by

See all 270

Metadata

Authors
Lutz, J.-F., Börner, H. G., & Weichenhan, K.
Venue
Macromolecules
Published
2006-08-19
Volume
39
Issue
19
Pages
6376-6383
ISSN
  • 0024-9297 (ISSN-L)
  • 1520-5835
OpenAlex
W2083881050
Cited by
270
References
2
FWCI
19.14
Type
journal article
Language
en
Open access
closed

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Combining ATRP and “Click” Chemistry: a Promising Platform toward Functional Biocompatible Polymers and Polymer Bioconjugates. https://app.cochat.ai/papers/10.1021/ma061557n
The paper
Lutz, J.-F., Börner, H. G., & Weichenhan, K. (2006). Combining ATRP and “Click” Chemistry: a Promising Platform toward Functional Biocompatible Polymers and Polymer Bioconjugates. Macromolecules. https://doi.org/10.1021/ma061557n

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.