Evidence map›Paper›PMID 39319032›Full record

ReviewBeilstein journal of organic chemistry2024

Asymmetric organocatalytic synthesis of chiral homoallylic amines.

Nikolay S Kondratyev, Andrei V Malkov

Abstract readReview
In one paragraph

Review in Beilstein journal of organic chemistry, 2024. 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. New advances in asymmetric organocatalysis II.Beilstein journal of organic chemistry · 2025
    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

2 authors.

Nikolay S KondratyevDepartment of Chemistry, Loughborough University, Loughborough, LE11 3TU, UK.ORCID https://orcid.org/0000-0001-6965-5302
Andrei V MalkovDepartment of Chemistry, Loughborough University, Loughborough, LE11 3TU, UK.ORCID https://orcid.org/0000-0001-6072-2353

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent decades, the chiral allylation of imines emerged as a key methodology in the synthesis of alkaloids and natural products with 4-, 5- and 6-membered cyclic amine motifs. Initially reliant on stoichiometric reagents, synthetic chemists predominantly used

Indexed as

asymmetric catalysisasymmetric synthesischiral aminesorganicatalysisrearrangement

Identifiers

PMID39319032
PMCPMC11420548

What Socratic 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 Socratic graph.