Evidence map›Paper›PMID 34522944›Full record

ArticleOrganic & biomolecular chemistry2021

Are bis(pyridine)iodine(I) complexes applicable for asymmetric halogenation?

Daniel von der Heiden, Flóra Boróka Németh, Måns Andreasson, Daniel Sethio, Imre Pápai, Mate Erdelyi

Abstract read
In one paragraph

Article in Organic & biomolecular chemistry, 2021. 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. Halogen Bonds of Halogen(I) Ions─Where Are We and Where to Go?Journal of the American Chemical Society · 2024
    Review
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.

Daniel von der HeidenDepartment of Chemistry - BMC, Uppsala University, SE-751 23 Uppsala, Sweden. mate.erdelyi@kemi.uu.se.ORCID http://orcid.org/0000-0003-4886-8696
Flóra Boróka NémethInstitute of Organic Chemistry, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Måns AndreassonDepartment of Chemistry and Molecular Biology, University of Gothenburg, SE-412 96 Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-8089-2333
Daniel SethioDepartment of Chemistry - BMC, Uppsala University, SE-751 23 Uppsala, Sweden. mate.erdelyi@kemi.uu.se.ORCID http://orcid.org/0000-0002-8075-1482
Imre PápaiInstitute of Organic Chemistry, Research Centre for Natural Sciences, H-1117 Budapest, Hungary.ORCID http://orcid.org/0000-0002-4978-0365
Mate ErdelyiDepartment of Chemistry - BMC, Uppsala University, SE-751 23 Uppsala, Sweden. mate.erdelyi@kemi.uu.se.ORCID http://orcid.org/0000-0003-0359-5970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enantiopure halogenated molecules are of tremendous importance as synthetic intermediates in the construction of pharmaceuticals, fragrances, flavours, natural products, pesticides, and functional materials. Enantioselective halofunctionalizations remain poorly understood and generally applicable procedures are lacking. The applicability of chiral

Identifiers

PMID34522944
PMCPMC8494190

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.