Evidence map›Paper›PMID 37800000›Full record

ArticleChemical science2023

Deaminative ring contraction for the synthesis of polycyclic heteroaromatics: a concise total synthesis of toddaquinoline.

Emily K Kirkeby, Zachary T Schwartz, Myles A Lovasz, Andrew G Roberts

Abstract read
In one paragraph

Article in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Journal of the American Chemical Society · 2024
    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.

Emily K KirkebyDepartment of Chemistry, University of Utah 315 South 1400 East Salt Lake City Utah 84112 USA roberts@chem.utah.edu.ORCID https://orcid.org/0000-0003-4080-7960
Zachary T SchwartzDepartment of Chemistry, University of Utah 315 South 1400 East Salt Lake City Utah 84112 USA roberts@chem.utah.edu.ORCID https://orcid.org/0009-0004-4331-1033
Myles A LovaszDepartment of Chemistry, University of Utah 315 South 1400 East Salt Lake City Utah 84112 USA roberts@chem.utah.edu.ORCID https://orcid.org/0009-0002-2173-2596
Andrew G RobertsDepartment of Chemistry, University of Utah 315 South 1400 East Salt Lake City Utah 84112 USA roberts@chem.utah.edu.ORCID https://orcid.org/0000-0002-2221-534X

Funding

Pd-Catalyzed Olefin Functionalization Reactions for Organic SynthesisR01GM063540 · NIGMS · UNIVERSITY OF UTAH · PI SIGMAN, MATTHEW S · 2002 to 2019
$5.3M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR017539 · NCRR · UNIVERSITY OF UTAH · PI PUGMIRE, RONALD J · 2003 to 2003
$3.8M
A 500MHz NMR Spectrometer with AutomationS10OD025241 · OD · UNIVERSITY OF UTAH · PI FLYNN, PETER F · 2018 to 2018
$600k
NCRR NIH HHS C06 RR017539NIGMS NIH HHS R01 GM063540NIH HHS S10 OD025241
6 · The paper itself

Abstract

A concise strategy to prepare polycyclic heteroaromatics involving a deaminative contraction cascade is detailed. The efficient deaminative ring contraction involves the

Identifiers

PMID37800000
PMCPMC10548534

What OpenQuestion holds

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LicenceCC BY-NC
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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.