Evidence map›Paper›PMID 38513032›Full record

ArticleScience (New York, N.Y.)2024

Alcohol-alcohol cross-coupling enabled by S

Ruizhe Chen, Nicholas E Intermaggio, Jiaxin Xie, James A Rossi-Ashton, Colin A Gould, Robert T Martin, Jesús Alcázar, David W C MacMillan

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

  1. Article
  2. Nickel-Catalyzed Radical-Radical Cross-Coupling Reactions.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Oxyalkylation of Alkenes via Triple Radical Sorting.Journal of the American Chemical Society · 2026
    Article
  10. Quaternary Carbons from Amines and Acids.Journal of the American Chemical Society · 2026
    Article
  11. Deaminative C(Journal of the American Chemical Society · 2026
    Article
  12. Nickel-Catalyzed Cross-Dehydrogenative Allylation of Aldehydes.Journal of the American Chemical Society · 2026
    Article
  13. Boron-Mediated Hydroalkylation of Unactivated Olefins: AnJournal of the American Chemical Society · 2026
    Article
  14. Article
  15. Article
  16. Intermolecular Cyclization of Alkyl Chains of Ketones for ConstructingJournal of the American Chemical Society · 2026
    Article
  17. Article
  18. Review
  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

8 authors.

Ruizhe Chen *Merck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0009-0002-3122-7550
Nicholas E Intermaggio *Merck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0009-0006-6193-6891
Jiaxin Xie *Merck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-5066-3553
James A Rossi-Ashton *Merck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-0989-2506
Colin A GouldMerck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0001-9539-1582
Robert T MartinMerck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-7676-2840
Jesús AlcázarDiscovery Chemistry, Janssen Research and Development, Janssen-Cilag, S.A., C/Jarama 75A, 45007 Toledo, Spain.ORCID 0000-0002-2726-196X
David W C MacMillanMerck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0001-6447-0587

Funding

Photoredox Catalysis Applications in Organometallics and Chemical BiologyR35GM134897 · NIGMS · PRINCETON UNIVERSITY · PI David W MacMillan · 2020 to 2026
$6.3M
NIGMS NIH HHS R35 GM134897
6 · The paper itself

Abstract

Alcohols represent a functional group class with unparalleled abundance and structural diversity. In an era of chemical synthesis that prioritizes reducing time to target and maximizing exploration of chemical space, harnessing these building blocks for carbon-carbon bond-forming reactions is a key goal in organic chemistry. In particular, leveraging a single activation mode to form a new C(sp

Identifiers

PMID38513032
PMCPMC11551712

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.