Evidence map›Paper›PMID 41614166›Full record

ArticleJACS Au2026

Polar-to-Radical Crossover in Catalyst-Free Olefin Halo-Hydroxylamination: A Direct Route to Multifunctional Electrophilic Hydroxylamines.

Young-Do Kwon, Daniel Joaquin, Michael T Davenport, Jeff Olsen, Melany Carpio, Muhammed Yousufuddin, Daniel H Ess, László Kürti

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in JACS Au, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Anomeric Amides: Valuable Reagents in Synthetic Organic Chemistry.Angewandte Chemie (International ed. in English) · 2026
    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

8 authors.

Young-Do KwonDepartment of Chemistry, Rice University, Houston, Texas 77030, United States.ORCID https://orcid.org/0000-0002-7515-6021
Daniel JoaquinDepartment of Chemistry, Rice University, Houston, Texas 77030, United States.ORCID https://orcid.org/0000-0002-7657-4743
Michael T DavenportDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.ORCID https://orcid.org/0000-0001-7483-5260
Jeff OlsenDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.
Melany CarpioDepartment of Natural Sciences, University of North Texas at Dallas, Dallas, Texas 75241, United States.
Muhammed YousufuddinDepartment of Natural Sciences, University of North Texas at Dallas, Dallas, Texas 75241, United States.ORCID https://orcid.org/0000-0002-4303-8303
Daniel H EssDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.ORCID https://orcid.org/0000-0001-5689-9762
László KürtiDepartment of Chemistry, Rice University, Houston, Texas 77030, United States.ORCID https://orcid.org/0000-0002-3412-5894

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we introduce a powerful alkene difunctionalization process where anomeric amides (i.e.,

Indexed as

alkene 1,2-difunctionalizationC−N bond formationC(sp2)−H aminationmultifunctional hydroxylaminesN-haloalkyl O-activated hydroxylaminesN-heterocyclesolefin aziridinationolefin halo-hydroxylamination

Identifiers

PMID41614166
PMCPMC12848737

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.