Evidence map›Paper›PMID 25233140›Full record

ArticleJournal of the American Chemical Society2014

Vicinal diamination of alkenes under Rh-catalysis.

David E Olson, Justin Y Su, D Allen Roberts, J Du Bois

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2014. 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. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. α-Diimine synthesisChemical science · 2022
    Article
  8. Photoinduced Olefin Diamination with Alkylamines.Angewandte Chemie (International ed. in English) · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  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

4 authors.

David E OlsonDepartment of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
Justin Y Su
D Allen Roberts
J Du Bois

Funding

Reaction Design for the Synthesis of Neuroactive AgentsR01NS045684 · NINDS · STANFORD UNIVERSITY · PI DU BOIS, JUSTIN · 2003 to 2011
$3.0M
NINDS NIH HHS R01 NS045684NINDS NIH HHS R01NS045684
6 · The paper itself

Abstract

The synthesis of 1,2-diamines has been achieved through a single-step, tandem sequence involving Rh-catalyzed aziridination followed by NaI-promoted rearrangement to an isomeric cyclic sulfamide. Facile ring opening of these products in hot water and pyridine affords differentially protected vicinal diamines. Demonstration of the utility of this method for the syntheses of (±)-enduracididine and (±)-allo-enduracididine is highlighted.

Indexed as

AlkenesAminationCatalysisDiaminesMolecular StructureOrganometallic CompoundsRhodiumAlkenesDiaminesOrganometallic CompoundsRhodium

Identifiers

PMID25233140
PMCPMC4183635

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.