Evidence map›Paper›PMID 42405091›Full record

ArticleRSC advances2026

Highly stereoselective synthesis of complex molecules

Max Benjamin Becker, Uli Kazmaier

Abstract read
In one paragraph

Article in RSC advances, 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

2 authors.

Max Benjamin BeckerOrganic Chemistry, Saarland University P.O. Box 151150 66041 Saarbrücken Germany u.kazmaier@mx.uni-saarland.de.
Uli KazmaierOrganic Chemistry, Saarland University P.O. Box 151150 66041 Saarbrücken Germany u.kazmaier@mx.uni-saarland.de.ORCID https://orcid.org/0000-0001-9756-0589

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matteson homologation not only allows the highly stereoselective synthesis of complex chiral boronic acid esters, but also the formation of chiral secondary alcohols through their oxidation. By converting them into chiral carbamates, they can be coupled with chiral boronic acid esters after deprotonation, whereby tertiary boronic acid esters can be obtained highly stereoselectively (d.r. ≥ 97 : 3). No matched/mismatched situation is observed,

Identifiers

PMID42405091
PMCPMC13331684

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.