Evidence map›Paper›PMID 40674771›Full record

ArticleThe Journal of organic chemistry2025

Selective Reductions of Esters to Aldehydes: Extended Scope and Downstream Reactivity.

Rebeka Ločmele, Gábor Szilvágyi, József Répási, Gints Smits

Abstract read
In one paragraph

Article in The Journal of organic chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Rebeka LočmeleLaboratory of CNS Active Compounds, Latvian Institute of Organic Synthesis, Aizkraukles 21, 1006 Riga, Latvia.
Gábor SzilvágyiAldexChem Ltd., Bajuszfu utca 59/A, 2030 Érd, Hungary.
József RépásiAldexChem Ltd., Bajuszfu utca 59/A, 2030 Érd, Hungary.
Gints SmitsLaboratory of CNS Active Compounds, Latvian Institute of Organic Synthesis, Aizkraukles 21, 1006 Riga, Latvia.ORCID 0000-0001-5044-4169

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In our study, we extended the applicability of ester hydrosilylation methodology employing (2-bromo-6-fluorophenyl)bis(2,3,5,6-tetrafluorophenyl)borane (SBR12) catalysts. Overall, the method features exceptionally low catalyst loading (as little as 0.01 mol %), along with mild reaction conditions and a high tolerance for various functional groups. We demonstrated the practicality of this technique through the concise total synthesis of the sex pheromone (

Identifiers

PMID40674771
PMCPMC12323772

What OpenQuestion holds

Textmetadata
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.