Evidence map›Paper›PMID 42175786›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2026

Flipping the Card With Enantiodivergent Organocatalysis.

Debora Iapadre, Alessio Carioscia, Alessandro Brusa, Armando Carlone

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. 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. Flipping the Card With Enantiodivergent Organocatalysis.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
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.

Debora IapadreDepartment of Physical and Chemical Sciences, Consorzio C.I.N.M.P.I.S., INSTM RU, Università degli Studi dell'Aquila, L'Aquila, Italy.
Alessio CariosciaDepartment of Physical and Chemical Sciences, Consorzio C.I.N.M.P.I.S., INSTM RU, Università degli Studi dell'Aquila, L'Aquila, Italy.
Alessandro BrusaDepartment of Physical and Chemical Sciences, Consorzio C.I.N.M.P.I.S., INSTM RU, Università degli Studi dell'Aquila, L'Aquila, Italy.
Armando CarloneDepartment of Physical and Chemical Sciences, Consorzio C.I.N.M.P.I.S., INSTM RU, Università degli Studi dell'Aquila, L'Aquila, Italy.

Funding

National Innovation Ecosystem ECS00000041-VITALITYPRIN 2022 PNRR ProjectP2022YM7F2
6 · The paper itself

Abstract

This minireview focuses on recent and most impactful contributions in enantiodivergent organocatalyzed reactions. Four different approaches based on achiral stimuli were examined as inversion strategies: solvent-controlled inversion, achiral reagent or additive-inducted inversion, and minimal catalyst modification, discussing in detail for each example the mechanistic insights behind the chiral inversion. Other strategies to achieve enantiodivergence are also briefly discussed.

Indexed as

achiral stimulienantiodivergenceorganocatalysis

Identifiers

PMID42175786
PMCPMC13451544

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.