Evidence map›Paper›PMID 24483250›Full record

ArticleOrganic letters2014

A concise synthesis of carolacton.

Michal S Hallside, Richard S Brzozowski, William M Wuest, Andrew J Phillips

Open access · bronzeAbstract read
In one paragraph

Article in Organic letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Collaboration in Natural Product Total Synthesis: Carolacton - A Decade of Discovery.Synlett : accounts and rapid communications in synthetic organic chemistry · 2021
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. 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

4 authors at 2 institutions in 1 country.

Michal S HallsideDepartment of Chemistry, Yale University , New Haven, Connecticut 06511, United States.
Richard S Brzozowski
William M Wuest
Andrew J Phillips
Temple University · USYale University · US

Funding

Total Synthesis of Bioactive CompoundsR01CA110246 · NCI · YALE UNIVERSITY · PI PHILLIPS, ANDREW J. · 2004 to 2013
$2.1M
Total Synthesis of Bioactive CompoundsR56CA110246 · NCI · UNIVERSITY OF COLORADO · PI PHILLIPS, ANDREW J. · 2009 to 2009
$225k
NCI NIH HHS CA110246NCI NIH HHS R01 CA110246NCI NIH HHS R56 CA110246
6 · The paper itself

Abstract

A synthesis of carolacton, a myxobacterial natural product that has profound effects on Streptococcus mutans biofilms, is reported. The synthesis proceeds via a longest linear sequence of 14 steps from an Evans β-ketoimide and enabled preliminary evaluations of the effects of late-stage intermediates on S. mutans biofilms. These studies suggest that further investigations into carolacton's structure-function relationships are warranted.

Indexed as

BiofilmsMacrolidesMolecular StructureMyxococcalesStreptococcus mutanscarolactonMacrolides

Identifiers

PMID24483250
PMCPMC3993612
OpenAlexW1973910136

What OpenQuestion holds

Textmetadata
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.