Evidence map›Paper›PMID 30155122›Full record

ArticleChemical science2016

Divergent enantioselective synthesis of hapalindole-type alkaloids using catalytic asymmetric hydrogenation of a ketone to construct the chiral core structure.

Yang Liu, Li-Jie Cheng, Hai-Tao Yue, Wen Che, Jian-Hua Xie, Qi-Lin Zhou

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Chemical science, 2016. 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. Review
  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

6 authors.

Yang LiuState Key Laboratory and Institute of Elemento-organic Chemistry , Nankai University , Tianjin 300071 , China . Email: jhxie@nankai.edu.cn.
Li-Jie ChengState Key Laboratory and Institute of Elemento-organic Chemistry , Nankai University , Tianjin 300071 , China . Email: jhxie@nankai.edu.cn.
Hai-Tao YueState Key Laboratory and Institute of Elemento-organic Chemistry , Nankai University , Tianjin 300071 , China . Email: jhxie@nankai.edu.cn.
Wen CheState Key Laboratory and Institute of Elemento-organic Chemistry , Nankai University , Tianjin 300071 , China . Email: jhxie@nankai.edu.cn.
Jian-Hua XieState Key Laboratory and Institute of Elemento-organic Chemistry , Nankai University , Tianjin 300071 , China . Email: jhxie@nankai.edu.cn.
Qi-Lin ZhouState Key Laboratory and Institute of Elemento-organic Chemistry , Nankai University , Tianjin 300071 , China . Email: jhxie@nankai.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A divergent enantioselective approach to hapalindole-type alkaloids is described. The route features a ruthenium-catalyzed asymmetric hydrogenation of a ketone

Identifiers

PMID30155122
PMCPMC6016446

What OpenQuestion holds

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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.