Evidence map›Paper›PMID 30759339›Full record

ArticleJournal of the American Chemical Society2019

Catalytic Strategy for Regioselective Arylethylamine Synthesis.

Allyson J Boyington, Ciaran P Seath, Avery M Zearfoss, Zihao Xu, Nathan T Jui

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Regiodivergent α- and β-Functionalization of SaturatedJournal of the American Chemical Society · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Photocatalytic Alkylation of C(spAngewandte Chemie (International ed. in English) · 2023
    Article
  12. Meerwein-type Bromoarylation with Arylthianthrenium Salts.Angewandte Chemie (International ed. in English) · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors.

Allyson J BoyingtonDepartment of Chemistry and Winship Cancer Institute , Emory University , Atlanta , Georgia 30322 , United States.
Ciaran P SeathDepartment of Chemistry and Winship Cancer Institute , Emory University , Atlanta , Georgia 30322 , United States.
Avery M ZearfossDepartment of Chemistry and Winship Cancer Institute , Emory University , Atlanta , Georgia 30322 , United States.
Zihao XuDepartment of Chemistry and Winship Cancer Institute , Emory University , Atlanta , Georgia 30322 , United States.
Nathan T JuiDepartment of Chemistry and Winship Cancer Institute , Emory University , Atlanta , Georgia 30322 , United States.ORCID 0000-0001-5315-0270

Funding

Novel Radical Reactions for C-C Bond FormationR01GM129495 · NIGMS · EMORY UNIVERSITY · PI BLAKEY, SIMON B. · 2018 to 2022
$1.5M
NIGMS NIH HHS R01 GM129495
6 · The paper itself

Abstract

A mild, modular, and practical catalytic system for the synthesis of the highly privileged phenethylamine pharmacophore is reported. Using a unique combination of organic catalysts to promote the transfer of electrons and hydrogen atoms, this system performs direct hydroarylation of vinyl amine derivatives with a wide range of aryl halides (including aryl chlorides). This general and highly chemoselective protocol delivers a broad range of arylethylamine products with complete regiocontrol. The utility of this process is highlighted by its scalability and the modular synthesis of an array of bioactive small molecules.

Identifiers

PMID30759339
PMCPMC6444931

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.