Evidence map›Paper›PMID 34368522›Full record

ReviewACS omega2021

Evolution of the Synthesis of Remdesivir. Classical Approaches and Most Recent Advances.

Didier F Vargas, Enrique L Larghi, Teodoro S Kaufman

Open access · goldAbstract readReview
In one paragraph

Review in ACS omega, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Enantioseparation ofMolecules (Basel, Switzerland) · 2023
    Article
  5. Total synthesis of remdesivir.Tetrahedron letters · 2022
    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 at 1 institution in 1 country.

Didier F VargasInstituto de Química Rosario (IQUIR, CONICET-UNR) and National University of Rosario (UNR), Suipacha 531, 2000 Rosario, Argentina.
Enrique L LarghiInstituto de Química Rosario (IQUIR, CONICET-UNR) and National University of Rosario (UNR), Suipacha 531, 2000 Rosario, Argentina.ORCID https://orcid.org/0000-0002-9791-4831
Teodoro S KaufmanInstituto de Química Rosario (IQUIR, CONICET-UNR) and National University of Rosario (UNR), Suipacha 531, 2000 Rosario, Argentina.ORCID https://orcid.org/0000-0003-3173-2178
Consejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The broad-spectrum antiviral Remdesivir, a monophosphate nucleoside analogue prodrug (ProTide), was repurposed. In May 2020, it received emergency approval by the FDA, being the first drug approved to fight the new coronavirus (COVID-19) disease which targets the virus directly. The main synthetic strategies toward Remdesivir, and their relevant modifications, are presented and discussed, to provide a panoramic view of the state-of-the-art and the more important advances in this field. Recent progress, proposed improvements, and uses of novel technologies for the synthetic sequence are also detailed.

Identifiers

PMID34368522
PMCPMC8340098
OpenAlexW3185895141

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.