Evidence map›Paper›PMID 38801413›Full record

ArticleJournal of the American Chemical Society2024

Regioselective Palladium-Catalyzed Chain-Growth Allylic Amination Polymerization of Vinyl Aziridines.

Jake R Jagannathan, Yutian Ma, Brennan J Curole, Scott M Grayson, Owen S Fenton, Frank A Leibfarth

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

6 authors.

Jake R JagannathanDepartment of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.
Yutian MaDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0002-0110-0244
Brennan J CuroleDepartment of Chemistry, Tulane University, 6400 Freret Street, 2015 Percival Stern Hall, New Orleans, Louisiana 70118, United States.
Scott M GraysonDepartment of Chemistry, Tulane University, 6400 Freret Street, 2015 Percival Stern Hall, New Orleans, Louisiana 70118, United States.ORCID 0000-0001-6345-8762
Owen S FentonDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0002-5585-9280
Frank A LeibfarthDepartment of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0001-7737-0331

Funding

CTSA K12 Program at UNCK12TR004416 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Michelle Hernandez, Jonathan J Juliano · 2023 to 2026
$6.5M
Stereoselective Polymerization Methods for the Synthesis of Degradable BiomaterialsR35GM142666 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LEIBFARTH, FRANK ALBERT · 2021 to 2025
$1.7M
NCATS NIH HHS K12 TR004416NIGMS NIH HHS R35 GM142666
6 · The paper itself

Abstract

Organometallic-mediated chain growth polymerization of readily accessible chemical building blocks is responsible for important commercial and technological advances in polymer science, but the incorporation of heteroatoms into the polymer backbone through these mechanisms remains a challenge. Transition metal π-allyl complexes are well-developed organometallic intermediates for carbon-heteroatom bond formation in small-molecule catalysis yet remain underexplored in polymer science. Here, we developed a regioselective palladium-phosphoramidite-catalyzed chain-growth allylic amination polymerization of vinyl aziridines for the synthesis of novel nitrogen-rich polymers via ambiphilic π-allyl complexes. The polymerization accessed a linear microstructure with four carbons between each nitrogen, which is challenging to achieve through other chain-growth polymerization approaches. The highly regioselective allylic amination polymerization demonstrated the characteristics of a controlled polymerization and was able to achieve molar masses exceeding 20 kg mol

Identifiers

PMID38801413
PMCPMC11977030

What OpenQuestion holds

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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.