Evidence map›Paper›PMID 32823507›Full record

ReviewMolecules (Basel, Switzerland)2020

Opening up the Toolbox: Synthesis and Mechanisms of Phosphoramidates.

Emeka J Itumoh, Shailja Data, Erin M Leitao

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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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.

Emeka J ItumohSchool of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.ORCID 0000-0001-5059-0529
Shailja DataSchool of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.
Erin M LeitaoSchool of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review covers the main synthetic routes to and the corresponding mechanisms of phosphoramidate formation. The synthetic routes can be separated into six categories: salt elimination, oxidative cross-coupling, azide, reduction, hydrophosphinylation, and phosphoramidate-aldehyde-dienophile (PAD). Examples of some important compounds synthesized through these routes are provided. As an important class of organophosphorus compounds, the applications of phosphoramidate compounds, are also briefly introduced.

Indexed as

AmidesChemistry Techniques, SyntheticPhosphoric AcidsAmidesphosphoramidic acidPhosphoric Acidsapplicationsmechanismphosphoramidatesynthetic routes

Identifiers

PMID32823507
PMCPMC7463754

What OpenQuestion holds

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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.