Evidence map›Paper›PMID 25753366›Full record

ArticleNature communications2015

Cobalt-catalysed site-selective intra- and intermolecular dehydrogenative amination of unactivated sp(3) carbons.

Xuesong Wu, Ke Yang, Yan Zhao, Hao Sun, Guigen Li, Haibo Ge

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Copper-Catalyzed γ-C(spAngewandte Chemie (International ed. in English) · 2025
    Article
  3. Synthesis of α-CFACS omega · 2023
    Article
  4. Article
  5. Ligand-Enabled β-C(spAngewandte Chemie (International ed. in English) · 2022
    Article
  6. Ligand Enabled Pd(II)-Catalyzed γ-C(spJournal of the American Chemical Society · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Co-catalyzedRSC advances · 2019
    Article
  14. Catalytic β C-H aminationChemical science · 2019
    Article
  15. Article
  16. Cobalt-catalyzed C(spRSC advances · 2018
    Article
  17. Article
  18. Complementary Strategies for Directed C(spAngewandte Chemie (International ed. in English) · 2018
    Review
  19. Review
  20. Catalytic Synthesis of N-Heterocycles via Direct C(spJournal of the American Chemical Society · 2017
    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

6 authors.

Xuesong WuDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University Indianapolis, 402 N. Blackford Street, Indianapolis, Indiana 46202, USA.
Ke YangInstitute of Chemistry and BioMedical Sciences, Nanjing University, Nanjing 210093, P.R. China.
Yan ZhaoDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University Indianapolis, 402 N. Blackford Street, Indianapolis, Indiana 46202, USA.
Hao SunInstitute of Chemistry and BioMedical Sciences, Nanjing University, Nanjing 210093, P.R. China.
Guigen Li1] Institute of Chemistry and BioMedical Sciences, Nanjing University, Nanjing 210093, P.R. China [2] Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409-1061, USA.
Haibo GeDepartment of Chemistry and Chemical Biology, Indiana University-Purdue University Indianapolis, 402 N. Blackford Street, Indianapolis, Indiana 46202, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cobalt-catalysed sp(2) C-H bond functionalization has attracted considerable attention in recent years because of the low cost of cobalt complexes and interesting modes of action in the process. In comparison, much less efforts have been devoted to the sp(3) carbons. Here we report the cobalt-catalysed site-selective dehydrogenative cyclization of aliphatic amides via a C-H bond functionalization process on unactivated sp(3) carbons with the assistance of a bidentate directing group. This method provides a straightforward synthesis of monocyclic and spiro β- or γ-lactams with good to excellent stereoselectivity and functional group tolerance. In addition, a new procedure has been developed to selectively remove the directing group, which enables the synthesis of free β- or γ-lactam compounds. Furthermore, the first cobalt-catalysed intermolecular dehydrogenative amination of unactivated sp(3) carbons is also realized.

Identifiers

PMID25753366
PMCPMC4366490

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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.