Evidence map›Paper›PMID 36778107›Full record

ArticleNational science review2022

Synthesis of pyrimidines from dinitrogen and carbon.

Xianghui Shi, Qianru Wang, Chao Qin, Li-Jun Wu, Yuanjin Chen, Gao-Xiang Wang, Yongli Cai, Wenbo Gao, Teng He, Junnian Wei and 3 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in National science review, 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. Conversion of NNature communications · 2025
    Article
  2. Review
  3. Chemical looping synthesis of amines from NNature communications · 2025
    Article
  4. Article
  5. 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

13 authors.

Xianghui ShiBeijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.
Qianru WangDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Chao QinDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Li-Jun WuBeijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.
Yuanjin ChenBeijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.
Gao-Xiang WangBeijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.
Yongli CaiDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Wenbo GaoDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Teng HeDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Junnian WeiBeijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.
Jianping GuoDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Ping ChenDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Zhenfeng XiBeijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.ORCID https://orcid.org/0000-0003-1124-5380

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The element nitrogen and nitrogenous compounds are vital to life. The synthesis of nitrogen-containing compounds using dinitrogen as the nitrogen source, not through ammonia, is of great interest and great value but remains a grand challenge. Herein, we describe a strategy to realize this transformation by combining the heterogeneous approach with the homogeneous methodology. The N

Indexed as

15n-labeled pyrimidinesdinitrogen transformationhomogeneous–heterogeneous synergy strategyN−C bond formationnitrogen fixation

Identifiers

PMID36778107
PMCPMC9905645

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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.