Evidence map›Paper›PMID 32012951›Full record

ReviewMolecules (Basel, Switzerland)2020

Nitroso Diels-Alder Cycloadducts Derived From

Andrea Menichetti, Francesco Berti, Mauro Pineschi

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

3 authors.

Andrea MenichettiDepartment of Pharmacy, University of Pisa, Via Bonanno 33, 56126 Pisa, Italy.
Francesco BertiDepartment of Pharmacy, University of Pisa, Via Bonanno 33, 56126 Pisa, Italy.
Mauro PineschiDepartment of Pharmacy, University of Pisa, Via Bonanno 33, 56126 Pisa, Italy.ORCID 0000-0001-6063-2198

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review focuses upon the use of nitroso Diels-Alder reactions as a structural complexity generating reaction that has been so far a quite scarcely treated topic, despite its potential. In particular, the use of

Indexed as

Cycloaddition ReactionCyclizationDihydropyridinesMolecular StructureNitroso CompoundsDihydropyridinesNitroso Compoundsdiversity oriented synthesisfunctionalized piperidinesfunctionalized pyrrolesheterobicyclic compoundsnitroso Diels-Alder

Identifiers

PMID32012951
PMCPMC7038088

What OpenQuestion holds

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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.