Evidence map›Paper›PMID 41959540›Full record

ReviewRSC chemical biology2026

Heck-type C-glycosylations in the synthesis of artificial nucleotides and functional nucleic acids.

Robert Dörrenhaus, Andre Zenz, Stephanie Kath-Schorr

Abstract readReview
In one paragraph

Review in RSC chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Robert DörrenhausUniversity of Cologne, Department of Chemistry and Biochemistry Greinstrasse 4 50939 Köln Germany skathsch@uni-koeln.de.ORCID https://orcid.org/0009-0006-4685-9939
Andre ZenzUniversity of Cologne, Department of Chemistry and Biochemistry Greinstrasse 4 50939 Köln Germany skathsch@uni-koeln.de.ORCID https://orcid.org/0000-0002-3516-2312
Stephanie Kath-SchorrUniversity of Cologne, Department of Chemistry and Biochemistry Greinstrasse 4 50939 Köln Germany skathsch@uni-koeln.de.ORCID https://orcid.org/0000-0002-5180-360X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in nucleic acid chemistry have driven the development of a wide variety of artificial nucleobases. The synthesis of the glycosidic bond towards nucleosides still remains a major challenge in nucleic acid chemistry, particularly for C-glycosidic DNA nucleosides. This review highlights the Heck reaction as a central and versatile strategy for constructing diverse C-glycosidic DNA analogues. It discusses the underlying reaction mechanism, commonly employed catalyst and ligand systems and the scope of tolerated substituents. In addition, the review summarizes the subsequent applications of these artificial nucleobases with a particular emphasis on fluorescent nucleobase analogues.

Identifiers

PMID41959540
PMCPMC13059217

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.