Evidence map›Paper›PMID 25146300›Full record

ArticleOrganic letters2014

Cobalt-catalyzed, aminoquinoline-directed coupling of sp(2) C-H bonds with alkenes.

Liene Grigorjeva, Olafs Daugulis

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Co-catalyzedRSC advances · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Aminoquinoline-directed, cobalt-catalyzed carbonylation of sulfonamide spChemical communications (Cambridge, England) · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

2 authors.

Liene GrigorjevaDepartment of Chemistry, University of Houston , Houston, Texas 77204-5003, United States.
Olafs Daugulis

Funding

New Methods for Direct Carbon-Hydrogen Bond FunctionalizationR01GM077635 · NIGMS · UNIVERSITY OF HOUSTON · PI DAUGULIS, OLAFS · 2007 to 2020
$3.6M
NIGMS NIH HHS R01 GM077635NIGMS NIH HHS R01GM077635
6 · The paper itself

Abstract

A method for cobalt-catalyzed, aminoquinoline-directed ortho-functionalization of sp(2) C-H bonds with alkenes has been developed. Reactions proceed at room temperature in trifluoroethanol solvent, use oxygen from air as an oxidant, and require Mn(OAc)3 as a cocatalyst. Benzoic, heteroaromatic, and acrylic acid aminoquinoline amides react with ethylene as well as mono- and disubstituted alkenes affording products in good yields. Excellent functional group tolerance is observed; halogen, nitro, ether, and unprotected alcohol functionalities are compatible with the reaction conditions.

Indexed as

AlkenesAminoquinolinesCatalysisCobaltCombinatorial Chemistry TechniquesMolecular StructureStereoisomerismAlkenesAminoquinolinesCobalt

Identifiers

PMID25146300
PMCPMC4155791

What OpenQuestion holds

Textmetadata
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.