Evidence map›Paper›PMID 31482682›Full record

ArticleAngewandte Chemie (International ed. in English)2019

Palladium-Catalyzed Dearomative syn-1,4-Oxyamination.

Conghui Tang, Mikiko Okumura, Hejun Deng, David Sarlah

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Chemical science · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Copper-Catalyzed Dearomative 1,2-Hydroamination.Angewandte Chemie (International ed. in English) · 2024
    Article
  6. Copper-Catalyzed DearomativeACS catalysis · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Pd-catalyzed allylative dearomatisation using Grignard reagents.Chemical communications (Cambridge, England) · 2021
    Article
  14. Lewis Acid Promoted Dearomatization of Naphthols.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020
    Article
  15. Article
  16. 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.

Conghui TangRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, IL 61801, USA.
Mikiko OkumuraRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, IL 61801, USA.
Hejun DengRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, IL 61801, USA.
David SarlahRoger Adams Laboratory, Department of Chemistry, University of Illinois, Urbana, IL 61801, USA.ORCID 0000-0002-8736-8953

Funding

Dearomative Functionalization with ArenophilesR01GM122891 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI SARLAH, DAVID · 2017 to 2025
$3.1M
Alfred P. Sloan FoundationAmerican Chemical Society Petroleum Research Fund PRF#57175-DNI1Directorate for Mathematical and Physical Sciences CHE-1654110NIGMS NIH HHS R01 GM122891
6 · The paper itself

Abstract

A palladium-catalyzed dearomative syn-1,4-oxyamination protocol using non-activated arenes has been developed. This one-pot procedure utilizes arenophile chemistry, and the corresponding para-cycloadducts are treated with oxygen nucleophiles via formal allylic substitution, providing direct access to syn-1,4-oxyaminated products. The reaction conditions permit a range of arenes, as well as different O-nucleophiles, such as oximes and benzyl alcohols. Moreover, this process was established in an asymmetric fashion, delivering products with high enantioselectivity. The dearomatized products are amenable to a multitude of further derivatizations ranging from olefin chemistry to C-H activation, giving rise to a diverse set of new functionalities. Overall, this dearomative functionalization offers rapid and controlled formation of molecular complexity, enabling straightforward access to functionalized small molecules from simple and readily available arenes.

Indexed as

Allyl CompoundsAminesCatalysisCycloaddition ReactionMolecular StructureOxygenPalladiumStereoisomerismAllyl CompoundsAminesOxygenPalladiumarenearenophiledearomatizationoxyaminationphotochemistry

Identifiers

PMID31482682
PMCPMC6803049

What OpenQuestion holds

Textmetadata
LicenceTDM
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.