Evidence map›Paper›PMID 38569596›Full record

ArticleJournal of the American Chemical Society2024

γ-Amino Alcohols via Energy Transfer Enabled Brook Rearrangement.

Ranjini Laskar, Subhabrata Dutta, Jan C Spies, Poulami Mukherjee, Ángel Rentería-Gómez, Daniel R. Thielemann, Constantin G Daniliuc, Osvaldo Gutierrez, Frank Glorius

Open access · hybridAbstract 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
17.0field-weighted citation impact, top 1% of its field
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

9 citing papers in PubMed, 68 citations in OpenAlex.

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  9. Catalytic Asymmetric Cycloaddition of Olefins with In Situ GeneratedJournal of the American Chemical Society · 2024
    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

9 authors at 2 institutions in 2 countries.

Ranjini LaskarOrganisch-Chemisches Institut, University of Münster, Corrensstrasse 36, 48149 Münster, Germany.
Subhabrata DuttaOrganisch-Chemisches Institut, University of Münster, Corrensstrasse 36, 48149 Münster, Germany.ORCID 0000-0002-6041-557X
Jan C SpiesOrganisch-Chemisches Institut, University of Münster, Corrensstrasse 36, 48149 Münster, Germany.ORCID 0009-0005-9793-6319
Poulami MukherjeeDepartment of Chemistry, Texas A&M University, 77843 College Station, Texas, United States.
Ángel Rentería-GómezDepartment of Chemistry, Texas A&M University, 77843 College Station, Texas, United States.
Daniel R. ThielemannOrganisch-Chemisches Institut, University of Münster, Corrensstrasse 36, 48149 Münster, Germany.
Constantin G DaniliucOrganisch-Chemisches Institut, University of Münster, Corrensstrasse 36, 48149 Münster, Germany.ORCID 0000-0002-6709-3673
Osvaldo GutierrezDepartment of Chemistry, Texas A&M University, 77843 College Station, Texas, United States.ORCID 0000-0001-8151-7519
Frank GloriusOrganisch-Chemisches Institut, University of Münster, Corrensstrasse 36, 48149 Münster, Germany.ORCID 0000-0002-0648-956X
University of Münster · DETexas A&M University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the long-standing quest to synthesize fundamental building blocks with key functional group motifs, photochemistry in the recent past has comprehensively established its attractiveness. Amino alcohols are not only functionally diverse but are ubiquitous in the biologically active realm of compounds. We developed bench-stable bifunctional reagents that could then access the sparsely reported γ-amino alcohols directly from feedstock alkenes through energy transfer (EnT) photocatalysis. A designed 1,3-linkage across alkenes is made possible by the intervention of a radical Brook rearrangement that takes place downstream to the EnT-mediated homolysis of our reagent(s). A combination of experimental mechanistic investigations and detailed computational studies (DFT) indicates a radical chain propagated reaction pathway.

Identifiers

PMID38569596
PMCPMC11027157
OpenAlexW4393903105

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.