Evidence map›Paper›PMID 35029626›Full record

ReviewOrganic & biomolecular chemistry2022

Synthetic and biosynthetic methods for selective cyclisations of 4,5-epoxy alcohols to tetrahydropyrans.

James I Bowen, Luoyi Wang, Matthew P Crump, Christine L Willis

Open access · hybridAbstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Organic & biomolecular chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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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 at 2 institutions in 2 countries.

James I BowenSchool of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK. chris.willis@bristol.ac.uk.ORCID 0000-0002-1596-4174
Luoyi WangCAS Key Laboratory of Microbial Physiological and Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0003-2032-7206
Matthew P CrumpSchool of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK. chris.willis@bristol.ac.uk.ORCID 0000-0002-7868-5818
Christine L WillisSchool of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK. chris.willis@bristol.ac.uk.ORCID 0000-0002-3919-3642
University of Bristol · GBChinese Academy of Sciences · CN

Funding

Biotechnology and Biological Sciences Research Council BB/L01386X/1
6 · The paper itself

Abstract

Tetrahydropyrans (THPs) are common structural motifs found in natural products and synthetic therapeutic molecules. In Nature these 6-membered oxygen heterocycles are often assembled

Indexed as

AlcoholsBiological ProductsEpoxy CompoundsPyransChemistry Techniques, SyntheticCyclizationMolecular StructureAlcoholsBiological ProductsEpoxy CompoundsPyrans

Identifiers

PMID35029626
PMCPMC8827043
OpenAlexW4205865338

What OpenQuestion holds

Textmetadata
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.