Evidence map›Paper›PMID 25198672›Full record

ArticleOrganic letters2014

Synthesis of substituted 2-aminoimidazoles via Pd-catalyzed alkyne carboamination reactions. Application to the synthesis of preclathridine natural products.

Blane P Zavesky, Nicholas R Babij, John P Wolfe

Abstract 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Catalytic Alkyne Arylation Using Traceless Directing Groups.Angewandte Chemie (International ed. in English) · 2018
    Article
  5. Article
  6. Article
  7. Article
  8. Total synthesis and cytotoxicity of Leucetta alkaloids.Bioorganic & medicinal chemistry · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Studies Towards theEuropean journal of organic chemistry · 2015
    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.

Blane P ZaveskyDepartment of Chemistry, University of Michigan , 930 North University Avenue, Ann Arbor, Michigan 48109-1005, United States.
Nicholas R Babij
John P Wolfe

Funding

New Reactions for Heterocycle SynthesisR01GM071650 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOLFE, JOHN P · 2005 to 2010
$1.2M
New Alkene Difunctionalization Reactions for Organic SynthesisR01GM098314 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOLFE, JOHN P · 2011 to 2014
$1.1M
NIGMS NIH HHS GM-071650NIGMS NIH HHS R01 GM071650NIGMS NIH HHS R01 GM098314
6 · The paper itself

Abstract

A new method for the synthesis of 2-aminoimidazole products is described. The heterocyclic products are generated in good yields via Pd-catalyzed carboamination reactions of N-propargyl guanidines and aryl triflates. This methodology generates both a C-N and C-C bond during the annulation step and facilitates the rapid construction of 2-aminoimidazole products with different aryl groups. The utility of this methodology was demonstrated in the total synthesis of preclathridine A, preclathridine B, and dorimidazole B from a single intermediate.

Indexed as

AlkaloidsBiological ProductsCombinatorial Chemistry TechniquesGuanidinesImidazolesMolecular StructurePalladium2-aminoimidazoleAlkaloidsBiological Productsclathridinedorimidazole BGuanidinesImidazolesPalladiumpreclathridine Apreclathridine B

Identifiers

PMID25198672
PMCPMC4168774

What OpenQuestion holds

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Registered trials

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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.