Evidence map›Paper›PMID 33623725›Full record

ArticleACS catalysis2020

Deuteration of Formyl Groups via a Catalytic Radical H/D Exchange Approach.

Yueteng Zhang, Peng Ji, Yue Dong, Yongyi Wei, Wei Wang

Open access · greenAbstract read
In one paragraph

Article in ACS catalysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 73 citations in OpenAlex.

  1. Water-Dispersible Ruthenium Nanocatalyst for Carbonyl Reduction With DAngewandte Chemie (International ed. in English) · 2026
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  6. Multiple remote C(spChemical science · 2022
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  11. Remote Site-Selective Radical C(spAngewandte Chemie (International ed. in English) · 2021
    Article
  12. Article
  13. Article
  14. 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

5 authors at 1 institution in 1 country.

Yueteng ZhangDepartment of Pharmacology and Toxicology, College of Pharmacy, and BIO5 Institute, University of Arizona, 1703 E. Mabel Street, Tucson, AZ 85721-0207, USA.
Peng JiDepartment of Pharmacology and Toxicology, College of Pharmacy, and BIO5 Institute, University of Arizona, 1703 E. Mabel Street, Tucson, AZ 85721-0207, USA.
Yue DongDepartment of Pharmacology and Toxicology, College of Pharmacy, and BIO5 Institute, University of Arizona, 1703 E. Mabel Street, Tucson, AZ 85721-0207, USA.
Yongyi WeiDepartment of Pharmacology and Toxicology, College of Pharmacy, and BIO5 Institute, University of Arizona, 1703 E. Mabel Street, Tucson, AZ 85721-0207, USA.
Wei WangDepartment of Pharmacology and Toxicology, College of Pharmacy, and BIO5 Institute, University of Arizona, 1703 E. Mabel Street, Tucson, AZ 85721-0207, USA.
University of Arizona · US

Funding

Organocatalytic Practical Synthesis of Deuterated Building Blocks and Biologically Important StructuresR01GM125920 · NIGMS · UNIVERSITY OF NEW MEXICO · PI WANG, WEI · 2018 to 2021
$1.2M
NIGMS NIH HHS R01 GM125920
6 · The paper itself

Abstract

H/D exchange at formyl groups represents the straightforward approach to C-1 deuterated aldehydes. This transformation has been recently realized by transition metal and NHC carbene catalysis. Mechanistically, all these processes involve an ionic pathway. Herein we report a distinct photoredox catalytic, visible light mediated neutral radical approach. Selective control of highly reactive acyl radical in the energy barrier surmountable, reversible reaction enables driving the formation of deuterated products when an excess of D

Indexed as

aldehydedeuterationH/D exchangephotoredoxradical reaction

Identifiers

PMID33623725
PMCPMC7899177
OpenAlexW3001619876

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.