Evidence map›Paper›PMID 35338143›Full record

ArticleNature communications2022

Kinetic resolution of cyclic benzylic azides enabled by site- and enantioselective C(sp

Pengbo Ye, Aili Feng, Lin Wang, Min Cao, Rongxiu Zhu, Lei Liu

Abstract read
In one paragraph

Article in Nature communications, 2022. 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. Article
  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

6 authors.

Pengbo Ye *School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Aili Feng *School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Lin Wang *School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Min CaoSchool of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Rongxiu ZhuSchool of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
Lei LiuSchool of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China. leiliu@sdu.edu.cn.ORCID http://orcid.org/0000-0002-0839-373X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Catalytic nonenzymatic kinetic resolution (KR) of racemates remains one of the most powerful tools to prepare enantiopure compounds, which dominantly relies on the manipulation of reactive functional groups. Moreover, catalytic KR of organic azides represents a formidable challenge due to the small size and instability of the azido group. Here, an effective KR of cyclic benzylic azides through site- and enantioselective C(sp

Indexed as

AzidesCatalysisKineticsOxidation-ReductionStereoisomerismAzides

Identifiers

PMID35338143
PMCPMC8956603

What OpenQuestion holds

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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.