Evidence map›Paper›PMID 42251636›Full record

ReviewChemistry, an Asian journal2026

Harnessing Molecular Strain to Program 1,2-Migration in Boronic Ester Chemistry.

Kanak Kanti Das

Abstract readReview
In one paragraph

Review in Chemistry, an Asian journal, 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

1 author.

Kanak Kanti DasKekulé-Institut Für Organische Chemie Und Biochemie, Rheinische Friedrich-Wilhelms-Universität, Bonn, Germany.ORCID https://orcid.org/0000-0002-9342-2709

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Strain in small-ring systems has emerged as a powerful intrinsic driver for stereospecific 1,2-metalate rearrangements in boronic ester chemistry, offering an alternative to classical electrophilic activation. By embedding stored strain energy within nitrogen-containing rings, cyclopropanes, epoxides, and bicyclo[1.1.0]butanes, otherwise disfavored carbon migrations can be selectively and predictably promoted. Release of this strain lowers activation barriers, enforces concerted pathways, and enables faithful transfer of stereochemical information from boron to carbon. Both transition-metal-mediated and metal-free triggers convert the latent strain into productive bond reorganization, allowing efficient access to complex, sp

Indexed as

1,2‐metalate rearrangementboronic estersskeletal reorganizationsmall‐ring activationstrain‐release chemistry

Identifiers

PMID42251636
PMCPMC13355104

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.