Evidence map›Paper›PMID 37298799›Full record

ArticleMolecules (Basel, Switzerland)2023

Organocatalytic Asymmetric Peroxidation of γ,δ-Unsaturated β-Keto Esters-A Novel Route to Chiral Cycloperoxides.

Mary C Hennessy, Hirenkumar Gandhi, Timothy P O'Sullivan

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. 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
0.4field-weighted citation impact, top 43% of its field
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, 3 citations in OpenAlex.

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

3 authors at 1 institution in 1 country.

Mary C HennessySchool of Chemistry, University College Cork, T12 YN60 Cork, Ireland.ORCID 0000-0001-6219-6107
Hirenkumar GandhiSchool of Chemistry, University College Cork, T12 YN60 Cork, Ireland.
Timothy P O'SullivanSchool of Chemistry, University College Cork, T12 YN60 Cork, Ireland.ORCID 0000-0001-6649-331X
University College Cork · IE

Funding

Irish Research Council GOIPG/2013/113Irish Research Council GOIPG/2018/496
6 · The paper itself

Abstract

A methodology for the asymmetric peroxidation of γ,δ-unsaturated β-keto esters is presented. Using a cinchona-derived organocatalyst, the target δ-peroxy-β-keto esters were obtained in high enantiomeric ratios of up to 95:5. Additionally, these δ-peroxy esters can be readily reduced to chiral δ-hydroxy-β-keto esters without impacting the β-keto ester functionality. Importantly, this chemistry opens up a concise route to chiral 1,2-dioxolanes, a common motif in many bioactive natural products, via a novel P

Indexed as

Biological ProductsDiet, KetogenicCatalysisEstersStereoisomerismBiological ProductsEsters1,2-dioxolanescycloperoxidesorganocatalysisδ-hydroxy-β-keto estersδ-peroxy-β-keto esters

Identifiers

PMID37298799
PMCPMC10254861
OpenAlexW4378228922

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.