Evidence map›Paper›PMID 35900638›Full record

ArticleMolecular diversity2024

New oxacycles on the block: benzodioxepinones via a Passerini reaction.

Michael Fragkiadakis, Marios Zingiridis, Edward Loukopoulos, Constantinos G Neochoritis

Abstract read
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In one paragraph

Article in Molecular diversity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Michael FragkiadakisDepartment of Chemistry, University of Crete, Heraklion, Greece.
Marios ZingiridisDepartment of Chemistry, University of Crete, Heraklion, Greece.
Edward LoukopoulosDepartment of Chemistry, University of Crete, Heraklion, Greece.
Constantinos G NeochoritisDepartment of Chemistry, University of Crete, Heraklion, Greece. kneochor@uoc.gr.ORCID http://orcid.org/0000-0001-5098-5504

Funding

Hellenic Foundation for Research and Innovation 911University of Crete ELKE
6 · The paper itself

Abstract

Oxacycles and benzoxepanes are privileged motifs present in a variety of natural products and functional molecules. However, their synthetic access is limited. Here, we demonstrate a rapid synthesis of unprecedented benzoxepanes from readily available starting materials in one step via a Passerini multicomponent reaction. The reaction proceeds smoothly under mild reaction conditions. We have obtained a single-crystal X-ray structure, revealing a butterfly conformation, combined with useful structural features. In addition, we have performed both a full interaction map on the X-ray structure and a profile analysis of a virtual library based on the proposed scaffold with a special focus on certain physicochemical parameters to demonstrate their potential usage in drug discovery.

Indexed as

Biological ProductsDrug DiscoveryMolecular StructureBiological ProductsDioxepinonesMulticomponent reactions (MCRs)OxacyclesPasserini reactionRule of five (Ro5)

Identifiers

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.