Evidence map›Paper›PMID 36091917›Full record

ArticleChemical science2022

Kinetic resolution of racemic tertiary allylic alcohols through S

Satavisha Kayal, Jun Kikuchi, Naoya Shinagawa, Shigenobu Umemiya, Masahiro Terada

Abstract read
In one paragraph

Article in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Satavisha KayalDepartment of Chemistry, Graduate School of Science, Tohoku University Aramaki, Aoba-ku Sendai 980-8578 Japan mterada@tohoku.ac.jp.
Jun KikuchiDepartment of Chemistry, Graduate School of Science, Tohoku University Aramaki, Aoba-ku Sendai 980-8578 Japan mterada@tohoku.ac.jp.ORCID https://orcid.org/0000-0001-9892-8832
Naoya ShinagawaDepartment of Chemistry, Graduate School of Science, Tohoku University Aramaki, Aoba-ku Sendai 980-8578 Japan mterada@tohoku.ac.jp.
Shigenobu UmemiyaDepartment of Chemistry, Graduate School of Science, Tohoku University Aramaki, Aoba-ku Sendai 980-8578 Japan mterada@tohoku.ac.jp.ORCID https://orcid.org/0000-0002-1793-856X
Masahiro TeradaDepartment of Chemistry, Graduate School of Science, Tohoku University Aramaki, Aoba-ku Sendai 980-8578 Japan mterada@tohoku.ac.jp.ORCID https://orcid.org/0000-0002-0554-8652

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A highly efficient kinetic resolution (KR) of racemic tertiary allylic alcohols was achieved through an intramolecular allylic substitution reaction using a co-catalyst system composed of chiral bisphosphoric acid and silver carbonate. This reaction afforded enantioenriched diene monoepoxides along with the recovery of tertiary allylic alcohols in a highly enantioselective manner, realizing an extremely high

Identifiers

PMID36091917
PMCPMC9400685

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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.