Evidence map›Paper›PMID 28178223›Full record

ReviewMolecules (Basel, Switzerland)2017

Recent Advances in Multinuclear NMR Spectroscopy for Chiral Recognition of Organic Compounds.

Márcio S Silva

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Article
  3. Recognition Mechanisms of Chiral Selectors: An Overview.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. A Thiourea Derivative of 2-[(1Molecules (Basel, Switzerland) · 2024
    Article
  9. (Molbank · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Thiourea Derivative of 2-[(1The Journal of organic chemistry · 2020
    Article
  16. RSC advances · 2020
    Article
  17. Article
  18. One-DimensionalMolecules (Basel, Switzerland) · 2018
    Article
  19. Article
  20. 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

1 author.

Márcio S SilvaCentro de Ciências Naturais e Humanas-CCNH-Universidade Federal do ABC-UFABC, Av. Dos Estados 5001, 09210-180 Santo André -SP, Brazil. s.marcio@ufabc.edu.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear magnetic resonance (NMR) is a powerful tool for the elucidation of chemical structure and chiral recognition. In the last decade, the number of probes, media, and experiments to analyze chiral environments has rapidly increased. The evaluation of chiral molecules and systems has become a routine task in almost all NMR laboratories, allowing for the determination of molecular connectivities and the construction of spatial relationships. Among the features that improve the chiral recognition abilities by NMR is the application of different nuclei. The simplicity of the multinuclear NMR spectra relative to ¹H, the minimal influence of the experimental conditions, and the larger shift dispersion make these nuclei especially suitable for NMR analysis. Herein, the recent advances in multinuclear (

Indexed as

Carboxylic AcidsCoordination ComplexesCyclodextrinsIonic LiquidsModels, MolecularMolecular ConformationNuclear Magnetic Resonance, BiomolecularPalladiumStereoisomerismCarboxylic AcidsCoordination ComplexesCyclodextrinsIonic LiquidsPalladiumabsolute configurationchiralitychiral recognitionenantiomeric excessenantiopuritymultinuclearNMR spectroscopystereochemistry

Identifiers

PMID28178223
PMCPMC6155827

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.