Evidence map›Paper›PMID 39364063›Full record

ArticleNature synthesis2024

Engineering non-haem iron enzymes for enantioselective C(sp3)-F bond formation via radical fluorine transfer.

Qun Zhao, Zhenhong Chen, Jordi Soler, Xiahe Chen, Jinyan Rui, Nathan Tianlin Ji, Qinglan E Yu, Yunfang Yang, Marc Garcia-Borràs, Xiongyi Huang

Abstract read
In one paragraph

Article in Nature synthesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
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  9. Examining Pseudohalide (NJournal of inorganic biochemistry · 2026
    Article
  10. Harnessing Photoenzymatic Systems for Intermolecular C-H Fluorination.Angewandte Chemie (International ed. in English) · 2026
    Article
  11. Article
  12. Non-heme iron enzymes step into the spotlight.Nature chemical biology · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Enantioconvergent benzylic C(spScience (New York, N.Y.) · 2025
    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

10 authors.

Qun ZhaoSchool of Biotechnology, Jiangnan University, Wuxi 214122, P. R. China.
Zhenhong ChenDepartment of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA.
Jordi SolerInstitut de Química Computacional i Catàlisi (IQCC) and Departament de Química, Universitat de Girona, Campus Montilivi, Girona E-17071, Catalonia, Spain.
Xiahe ChenState Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Key Laboratory of Green Chemistry-Synthesis Technology of Zhejiang Province, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, China.
Jinyan RuiDepartment of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA.
Nathan Tianlin JiDepartment of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA.
Qinglan E YuThe Bryn Mawr School, Baltimore, MD 21210, USA.
Yunfang YangState Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Key Laboratory of Green Chemistry-Synthesis Technology of Zhejiang Province, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, China.
Marc Garcia-BorràsInstitut de Química Computacional i Catàlisi (IQCC) and Departament de Química, Universitat de Girona, Campus Montilivi, Girona E-17071, Catalonia, Spain.
Xiongyi HuangDepartment of Chemistry, Johns Hopkins University, Baltimore, MD 21218, USA.

Funding

A Chemo-Mimetic Platform to Reprogram Metalloenzymes for Non-Natural Biocatalytic C-H Functionalization ReactionsR35GM147639 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Xiongyi Huang · 2022 to 2026
$2.1M
Expanding the chemistry of life: New enzymatic platforms for synthesis of bioactive organofluorinesR00GM129419 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI HUANG, XIONGYI · 2020 to 2022
$747k
NIGMS NIH HHS R00 GM129419NIGMS NIH HHS R35 GM147639
6 · The paper itself

Abstract

In recent years there has been a surge in the development of methods for the synthesis of organofluorine compounds. However, enzymatic methods for C-F bond formation have been limited to nucleophilic fluoride substitution. Here, we report the incorporation of iron-catalysed radical fluorine transfer, a reaction mechanism that is not used in naturally occurring enzymes, into enzymatic catalysis for the development of biocatalytic enantioselective C(

Identifiers

PMID39364063
PMCPMC11446476

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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.