Evidence map›Paper›PMID 42681709›Full record

ArticleThe Journal of organic chemistry2026

Reductive Deoxygenation of Aromatic Aldehydes and Ketones with Boron Triiodide.

Thomas M Chiarella, Anthony P Furrule, Florence J Williams

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 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.

Thomas M ChiarellaUniversity of Iowa , Iowa City, Iowa52246, United States.
Anthony P FurruleUniversity of Iowa , Iowa City, Iowa52246, United States.
Florence J WilliamsUniversity of Iowa , Iowa City, Iowa52246, United States.ORCID 0000-0003-2416-3843

Funding

Division of Chemistry CHE 2239556
6 · The paper itself

Abstract

Deoxygenation of carbonyls is an area of value in synthetic transformations because it allows for the traceless utilization of carbonyl chemistry, a mainstay in synthetic manipulations. Since oxygenation patterns are common in biological settings, deoxygenation can also be used to valorize biologically derived feedstocks. Herein, we describe the use of potassium borohydride and iodine, two common and benchtop-stable reagents, to generate boron triiodide in situ, which performs full deoxygenation of aryl aldehydes and ketones. For aldehydes, benzyl iodide products are formed, whereas for ketones, the fully reduced methylene is produced. Byproducts upon workup are low-toxicity boric acid and iodide salts, making the process practical and appealing for a wide range of applications.

Identifiers

PMID42681709
PMCPMC13532174

What OpenQuestion holds

Textmetadata
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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.