Evidence map›Paper›PMID 41554639›Full record

ArticleOrganic letters2026

Serendipity-Driven Telescoped Synthesis of 2-Aryl Glycidic Esters from Aldehydes.

Vincenzo Battaglia, Isaac G Sonsona, Sara Meninno, Carlo Crescenzi, Alessandra Lattanzi

Abstract read
In one paragraph

Article in Organic letters, 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

5 authors.

Vincenzo BattagliaDipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Italy.
Isaac G SonsonaDipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Italy.
Sara MeninnoDipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Italy.ORCID 0000-0001-8364-0211
Carlo CrescenziDipartimento di Farmacia, Università di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Italy.ORCID 0000-0001-6950-1506
Alessandra LattanziDipartimento di Chimica e Biologia "A. Zambelli", Università di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Italy.ORCID 0000-0003-1132-8610

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A first general and practical method for the synthesis of valuable 2-(hetero)aryl glycidic ethyl esters has been developed using commercially available reagents and a catalyst. A telescoped three-step seven-reaction process, based on a Knoevenagel/nitro-Michael/hydroxylation/double elimination/epoxidation/esterification sequence, provides the epoxides in up to 73% overall yield. This one-pot protocol features (i) aldehydes as versatile feedstocks, among the reagents used in the process; (ii) all steps proceeding at room temperature in benign solvents; and (iii) scalability of the reaction up to 5 mmol. The epoxides are elaborated to obtain new attractive β-amino α-hydroxy esters, bearing a quaternary stereocenter, including tryptamine- and morpholine-based esters.

Identifiers

PMID41554639
PMCPMC12865760

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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.