Evidence map›Paper›PMID 37175086›Full record

ArticleMolecules (Basel, Switzerland)2023

Ruthenium-Catalyzed Oxidative Synthesis of N-(2-triazine)indoles by C-H Activation.

Ming Zeng, Jiaqi Chen, Fengye Li, Haojie Li, Lan Zhao, Dengzhao Jiang, Jun Dai, Wenbo Liu

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 1 institution in 1 country.

Ming ZengSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.ORCID 0000-0002-4049-1815
Jiaqi ChenSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Fengye LiSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Haojie LiSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Lan ZhaoSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Dengzhao JiangSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Jun DaiSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Wenbo LiuSchool of Pharmacy and Life Science, Jiujiang University, Jiujiang 332005, China.
Jiujiang University · CN

Funding

Natural Science Foundation of China 21967013Natural Science Foundation of Jiangxi province 20212BAB216070Natural Science Foundation of Jiangxi province 20224BAB206119The Foundation of Jiangxi Provincial Department of Education GJJ201825The Foundation of Jiangxi Provincial Department of Education GJJ2201931
6 · The paper itself

Abstract

1,3,5 triazines, especially indole functionalized triazine derivatives, exhibit excellent activities, such as anti-tumor, antibacterial, and anti-inflammatory activities. Traditional methods for the synthesis of N-(2-triazine) indoles suffer from unstable materials and tedious operations. Transition-metal-catalyzed C-C/C-N coupling provides a powerful protocol for the synthesis of indoles by the C-H activation strategy. Here, we report the efficient ruthenium-catalyzed oxidative synthesis of N-(2-triazine) indoles by C-H activation from alkynes and various substituted triazine derivatives in a moderate to good yield, and all of the N-(2-triazine) indoles were characterized by

Indexed as

C-H activationindolesrutheniumtriazines

Identifiers

PMID37175086
PMCPMC10179826
OpenAlexW4366833550

What OpenQuestion holds

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LicenceCC BY
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.