Evidence map›Paper›PMID 28989660›Full record

ArticleChemical science2017

Rh-catalyzed aerobic oxidative cyclization of anilines, alkynes, and CO.

Xinyao Li, Jun Pan, Hao Wu, Ning Jiao

Abstract read
In one paragraph

Article in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

4 authors.

Xinyao LiState Key Laboratory of Natural and Biomimetic Drugs , Peking University , School of Pharmaceutical Sciences , Xue Yuan Rd. 38 , Beijing 100191 , China . Email: jiaoning@pku.edu.cn.
Jun PanState Key Laboratory of Natural and Biomimetic Drugs , Peking University , School of Pharmaceutical Sciences , Xue Yuan Rd. 38 , Beijing 100191 , China . Email: jiaoning@pku.edu.cn.
Hao WuState Key Laboratory of Natural and Biomimetic Drugs , Peking University , School of Pharmaceutical Sciences , Xue Yuan Rd. 38 , Beijing 100191 , China . Email: jiaoning@pku.edu.cn.
Ning JiaoState Key Laboratory of Natural and Biomimetic Drugs , Peking University , School of Pharmaceutical Sciences , Xue Yuan Rd. 38 , Beijing 100191 , China . Email: jiaoning@pku.edu.cn.ORCID 0000-0003-0290-9034

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transition-metal-catalyzed oxidative C-H cyclization of anilines has been an attractive and powerful strategy for the efficient construction of N-heterocycles. However, primary and tertiary anilines are rarely employed in this strategy due to the relative instability with strong oxidants or the presence of three C-N bonds. We describe here a novel Rh-catalyzed C-H cyclization of a wide range of anilines with alkynes and CO, using an aerobic oxidative protocol. Particularly, the simple primary anilines and readily prepared tertiary anilines could be easily converted to quinolin-2(1

Identifiers

PMID28989660
PMCPMC5628386

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.