Evidence map›Paper›PMID 34122935›Full record

ArticleChemical science2020

Exploiting the radical reactivity of diazaphosphinanes in hydrodehalogenations and cascade cyclizations.

Jingjing Zhang, Jin-Dong Yang, Jin-Pei Cheng

Abstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 1,3,2-Diazaphospholene-Catalyzed Reductive Cyclizations of Organohalides.Angewandte Chemie (International ed. in English) · 2022
    Article
  5. Article
  6. 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

3 authors.

Jingjing ZhangCenter of Basic Molecular Science, Department of Chemistry, Tsinghua University Beijing 100084 China jdyang@mail.tsinghua.edu.cn jinpei_cheng@mail.tsinghua.edu.cn.
Jin-Dong YangCenter of Basic Molecular Science, Department of Chemistry, Tsinghua University Beijing 100084 China jdyang@mail.tsinghua.edu.cn jinpei_cheng@mail.tsinghua.edu.cn.ORCID https://orcid.org/0000-0001-7351-2152
Jin-Pei ChengCenter of Basic Molecular Science, Department of Chemistry, Tsinghua University Beijing 100084 China jdyang@mail.tsinghua.edu.cn jinpei_cheng@mail.tsinghua.edu.cn.ORCID https://orcid.org/0000-0001-8822-1577

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The remarkable reducibility of diazaphosphinanes has been extensively applied in various hydrogenations, based on and yet limited by their well-known hydridic reactivity. Here we exploited their unprecedented radical reactivity to implement hydrodehalogenations and cascade cyclizations originally inaccessible by hydride transfer. These reactions feature a broad substrate scope, high efficiency and simplicity of manipulation. Mechanistic studies suggested a radical chain process in which a phosphinyl radical is generated in a catalytic cycle

Identifiers

PMID34122935
PMCPMC8159257

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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.