Evidence map›Paper›PMID 28154075›Full record

ArticleScience (New York, N.Y.)2017

Formation of α-chiral centers by asymmetric β-C(sp3)-H arylation, alkenylation, and alkynylation.

Qing-Feng Wu, Peng-Xiang Shen, Jian He, Xiao-Bing Wang, Forrest Zhang, Qian Shao, Ru-Yi Zhu, Claudio Mapelli, Jennifer X Qiao, Michael A Poss and 1 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
14.5field-weighted citation impact, top 1% of its field
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

58 citing papers in PubMed, 211 citations in OpenAlex.

  1. Ligand-Enabled Stereoselective Coupling of Methylene C(spAngewandte Chemie (International ed. in English) · 2026
    Article
  2. Pd(II)-Catalyzed Strategies for the β-Arylation of α-Amino Acids: An Overview.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  3. Intermolecular Enantioselective Nickel-Catalyzed Arylation of Un-Activated C(spAngewandte Chemie (International ed. in English) · 2026
    Article
  4. Article
  5. Conformation-driven C3-C(Nature catalysis · 2026
    Article
  6. Transition-Metal-Catalyzed C(spTopics in current chemistry (Cham) · 2025
    Review
  7. Enantioselective β-C(spJournal of the American Chemical Society · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Organic letters · 2024
    Article
  12. Article
  13. Vitamin BRSC advances · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Ligand-Enabled β-C(spAngewandte Chemie (International ed. in English) · 2022
    Article
  19. Palladium-Catalyzed Enantioselective β-C(spAccounts of chemical research · 2022
    Article
  20. Review
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

11 authors at 1 institution in 1 country.

Qing-Feng WuThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Peng-Xiang ShenThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Jian HeThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Xiao-Bing WangThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Forrest ZhangThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Qian ShaoThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Ru-Yi ZhuThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Claudio MapelliDiscovery Chemistry, Research and Development, Bristol-Myers Squibb Company, P.O. Box 4000, Princeton, NJ 08543, USA.
Jennifer X QiaoDiscovery Chemistry, Research and Development, Bristol-Myers Squibb Company, P.O. Box 4000, Princeton, NJ 08543, USA.
Michael A PossDiscovery Chemistry, Research and Development, Bristol-Myers Squibb Company, P.O. Box 4000, Princeton, NJ 08543, USA.
Jin-Quan YuThe Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. yu200@scripps.edu.
Scripps Research Institute · US

Funding

Ligand-promoted Enantioselective C-H Activation ReactionsR01GM084019 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI YU, JIN-QUAN · 2008 to 2024
$9.5M
NIGMS NIH HHS R01 GM084019
6 · The paper itself

Abstract

The enzymatic β-C-H hydroxylation of the feedstock chemical isobutyric acid has enabled the asymmetric synthesis of a wide variety of polyketides. The analogous transition metal-catalyzed enantioselective β-C-H functionalization of isobutyric acid-derived substrates should provide a versatile method for constructing useful building blocks with enantioenriched α-chiral centers from this abundant C-4 skeleton. However, the desymmetrization of ubiquitous isopropyl moieties by organometallic catalysts has remained an unanswered challenge. Herein, we report the design of chiral mono-protected aminomethyl oxazoline ligands that enable desymmetrization of isopropyl groups via palladium insertion into the C(sp

Identifiers

PMID28154075
PMCPMC5480404
OpenAlexW2583627348

What OpenQuestion holds

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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.