Evidence map›Paper›PMID 35974749›Full record

ArticleChemical science2022

Catalytic enantioselective synthesis of fluoromethylated stereocenters by asymmetric hydrogenation.

Jianping Yang, Sudipta Ponra, Xingzhen Li, Bram B C Peters, Luca Massaro, Taigang Zhou, Pher G Andersson

Abstract read
In one paragraph

Article in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. On the Nature of Improper Hydrogen Bonding in RCHAngewandte Chemie (International ed. in English) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. 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

7 authors.

Jianping YangDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory 106 91 Stockholm Sweden pher.andersson@su.se.
Sudipta PonraDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory 106 91 Stockholm Sweden pher.andersson@su.se.
Xingzhen LiCollege of Chemistry and Chemical Engineering, Southwest Petroleum University Chengdu Sichuan 610500 China tgzhou@swpu.edu.cn.
Bram B C PetersDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory 106 91 Stockholm Sweden pher.andersson@su.se.ORCID https://orcid.org/0000-0001-7788-3866
Luca MassaroDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory 106 91 Stockholm Sweden pher.andersson@su.se.ORCID https://orcid.org/0000-0001-6806-6039
Taigang ZhouCollege of Chemistry and Chemical Engineering, Southwest Petroleum University Chengdu Sichuan 610500 China tgzhou@swpu.edu.cn.ORCID https://orcid.org/0000-0002-3208-067X
Pher G AnderssonDepartment of Organic Chemistry, Stockholm University, Arrhenius Laboratory 106 91 Stockholm Sweden pher.andersson@su.se.ORCID https://orcid.org/0000-0002-1383-8246

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluoromethyl groups possess specific steric and electronic properties and serve as a bioisostere of alcohol, thiol, nitro, and other functional groups, which are important in an assortment of molecular recognition processes. Herein we report a catalytic method for the asymmetric synthesis of a variety of enantioenriched products bearing fluoromethylated stereocenters with excellent yields and enantioselectivities. Various N,P-ligands were designed and applied in the hydrogenation of fluoromethylated olefins and vinyl fluorides.

Identifiers

PMID35974749
PMCPMC9337738

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Registered trials

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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.