Evidence map›Paper›PMID 29147517›Full record

ArticleChemical science2017

Ketones as directing groups in photocatalytic sp

Desta Doro Bume, Cody Ross Pitts, Fereshte Ghorbani, Stefan Andrew Harry, Joseph N Capilato, Maxime A Siegler, Thomas Lectka

Abstract read
In one paragraph

Article in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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

7 authors.

Desta Doro BumeDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.
Cody Ross PittsDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.ORCID 0000-0003-1047-8924
Fereshte GhorbaniDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.
Stefan Andrew HarryDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.
Joseph N CapilatoDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.
Maxime A SieglerDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.
Thomas LectkaDepartment of Chemistry , Johns Hopkins University , 3400 N. Charles St. , Baltimore , MD 21218 , USA . Email: lectka@jhu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ubiquitous ketone carbonyl group generally deactivates substrates toward radical-based fluorinations, especially sites closest to it. Herein, ketones are used instead to direct aliphatic fluorination using Selectfluor, catalytic benzil, and visible light. Selective β- and γ-fluorination are demonstrated on rigid mono-, di-, tri-, and tetracyclic (steroidal) substrates employing both cyclic and exocyclic aliphatic ketones as directing groups.

Identifiers

PMID29147517
PMCPMC5637129

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.